Run ID: SRR3675283
Sample name:
Date: 04-04-2023 05:25:41
Number of reads: 22150
Percentage reads mapped: 8.52
Strain: lineage4.9
Drug-resistance: Sensitive
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|---|---|---|---|
| lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
| lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrA | 6727 | c.-575G>T | upstream_gene_variant | 1.0 |
| gyrA | 6728 | c.-574_-572delCTAinsTTG | upstream_gene_variant | 1.0 |
| gyrA | 6745 | c.-557T>C | upstream_gene_variant | 1.0 |
| gyrA | 6754 | c.-548C>T | upstream_gene_variant | 1.0 |
| gyrA | 6763 | c.-539G>C | upstream_gene_variant | 1.0 |
| gyrA | 6775 | c.-527G>C | upstream_gene_variant | 1.0 |
| gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
| gyrB | 6798 | p.Gly520Ala | missense_variant | 1.0 |
| gyrA | 6808 | c.-494C>A | upstream_gene_variant | 1.0 |
| gyrA | 6811 | c.-491C>T | upstream_gene_variant | 1.0 |
| gyrA | 6824 | c.-478C>T | upstream_gene_variant | 1.0 |
| gyrA | 6841 | c.-461T>C | upstream_gene_variant | 1.0 |
| gyrA | 6862 | c.-440C>G | upstream_gene_variant | 1.0 |
| gyrB | 7051 | p.Glu604Asp | missense_variant | 1.0 |
| gyrA | 7066 | c.-236G>T | upstream_gene_variant | 1.0 |
| gyrA | 7081 | c.-221T>C | upstream_gene_variant | 1.0 |
| gyrA | 7084 | c.-218A>G | upstream_gene_variant | 1.0 |
| gyrA | 7090 | c.-212C>T | upstream_gene_variant | 1.0 |
| gyrA | 7093 | c.-209T>C | upstream_gene_variant | 1.0 |
| gyrA | 7100 | c.-202T>C | upstream_gene_variant | 1.0 |
| gyrA | 7123 | c.-179C>G | upstream_gene_variant | 1.0 |
| gyrA | 7126 | c.-176G>C | upstream_gene_variant | 1.0 |
| gyrA | 7129 | c.-173T>G | upstream_gene_variant | 1.0 |
| gyrA | 7132 | c.-170T>C | upstream_gene_variant | 1.0 |
| gyrA | 7135 | c.-167G>A | upstream_gene_variant | 1.0 |
| gyrA | 7136 | c.-166T>C | upstream_gene_variant | 1.0 |
| gyrA | 7141 | c.-161T>G | upstream_gene_variant | 1.0 |
| gyrA | 7144 | c.-158A>G | upstream_gene_variant | 1.0 |
| gyrA | 7150 | c.-152G>A | upstream_gene_variant | 1.0 |
| gyrA | 7153 | c.-149G>C | upstream_gene_variant | 1.0 |
| gyrA | 7168 | c.-134C>G | upstream_gene_variant | 1.0 |
| gyrA | 7178 | c.-124T>C | upstream_gene_variant | 1.0 |
| gyrA | 7186 | c.-116C>G | upstream_gene_variant | 1.0 |
| gyrA | 7189 | c.-113C>T | upstream_gene_variant | 1.0 |
| gyrA | 7198 | c.-104C>T | upstream_gene_variant | 1.0 |
| gyrB | 7210 | p.Asp657Glu | missense_variant | 1.0 |
| gyrA | 7511 | c.210C>T | synonymous_variant | 1.0 |
| gyrA | 7523 | c.222C>G | synonymous_variant | 1.0 |
| gyrA | 7526 | c.225G>C | synonymous_variant | 1.0 |
| gyrA | 7547 | c.246C>T | synonymous_variant | 1.0 |
| gyrA | 7559 | c.258G>C | synonymous_variant | 1.0 |
| gyrA | 7565 | c.264C>T | synonymous_variant | 1.0 |
| gyrA | 7574 | c.273G>C | synonymous_variant | 1.0 |
| gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
| gyrA | 7589 | c.288G>C | synonymous_variant | 1.0 |
| gyrA | 7595 | c.294C>T | synonymous_variant | 1.0 |
| gyrA | 7607 | c.306C>T | synonymous_variant | 1.0 |
| gyrA | 7637 | c.336C>A | synonymous_variant | 1.0 |
| gyrA | 7655 | c.354G>A | synonymous_variant | 1.0 |
| gyrA | 7658 | c.357A>G | synonymous_variant | 1.0 |
| gyrA | 8915 | c.1614A>G | synonymous_variant | 1.0 |
| rpoB | 760139 | c.333A>G | synonymous_variant | 1.0 |
| rpoB | 760181 | c.375T>C | synonymous_variant | 1.0 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760196 | c.390C>G | synonymous_variant | 1.0 |
| rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
| rpoB | 760460 | c.654G>C | synonymous_variant | 1.0 |
| rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
| rpoB | 760481 | c.675G>T | synonymous_variant | 1.0 |
| rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
| rpoB | 760502 | c.696C>G | synonymous_variant | 1.0 |
| rpoB | 760522 | p.Ser239Asn | missense_variant | 1.0 |
| rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
| rpoB | 760541 | c.735G>C | synonymous_variant | 1.0 |
| rpoB | 761555 | c.1749G>C | synonymous_variant | 1.0 |
| rpoB | 761558 | c.1752C>G | synonymous_variant | 1.0 |
| rpoB | 761564 | c.1758G>C | synonymous_variant | 1.0 |
| rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
| rpoB | 761579 | c.1773G>C | synonymous_variant | 1.0 |
| rpoB | 761606 | c.1800C>G | synonymous_variant | 1.0 |
| rpoB | 761612 | c.1806G>T | synonymous_variant | 1.0 |
| rpoB | 761615 | c.1809A>C | synonymous_variant | 1.0 |
| rpoB | 761636 | c.1830G>T | synonymous_variant | 1.0 |
| rpoB | 761645 | c.1839C>G | synonymous_variant | 1.0 |
| rpoB | 761648 | c.1842T>C | synonymous_variant | 1.0 |
| rpoB | 761660 | c.1854G>T | synonymous_variant | 1.0 |
| rpoB | 761669 | c.1863C>T | synonymous_variant | 1.0 |
| rpoB | 761675 | c.1869G>C | synonymous_variant | 1.0 |
| rpoB | 761687 | c.1881C>T | synonymous_variant | 1.0 |
| rpoB | 761690 | c.1884G>C | synonymous_variant | 1.0 |
| rpoB | 761693 | c.1887G>C | synonymous_variant | 1.0 |
| rpoB | 761705 | c.1899C>A | synonymous_variant | 1.0 |
| rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762194 | c.2388G>C | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
| rpoB | 762236 | c.2430G>C | synonymous_variant | 1.0 |
| rpoB | 762239 | c.2433G>A | synonymous_variant | 1.0 |
| rpoB | 762245 | c.2439G>C | synonymous_variant | 1.0 |
| rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
| rpoB | 762275 | c.2469C>T | synonymous_variant | 1.0 |
| rpoB | 762284 | c.2478G>C | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762296 | c.2490G>C | synonymous_variant | 1.0 |
| rpoB | 762314 | c.2508C>T | synonymous_variant | 1.0 |
| rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
| rpoB | 762323 | c.2517C>A | synonymous_variant | 1.0 |
| rpoB | 762329 | c.2523G>C | synonymous_variant | 1.0 |
| rpoB | 762338 | c.2532T>C | synonymous_variant | 1.0 |
| rpoB | 762341 | c.2535G>C | synonymous_variant | 1.0 |
| rpoB | 762347 | c.2541T>C | synonymous_variant | 1.0 |
| rpoB | 762350 | c.2544C>G | synonymous_variant | 1.0 |
| rpoB | 762353 | c.2547C>T | synonymous_variant | 1.0 |
| rpoB | 762356 | p.Glu850Asp | missense_variant | 1.0 |
| rpoB | 762362 | p.Glu852Asp | missense_variant | 1.0 |
| rpoB | 762368 | p.Glu854Asp | missense_variant | 1.0 |
| rpoB | 762369 | c.2563T>C | synonymous_variant | 1.0 |
| rpoC | 762374 | c.-996G>T | upstream_gene_variant | 1.0 |
| rpoC | 762380 | c.-990T>C | upstream_gene_variant | 1.0 |
| rpoC | 762383 | c.-987C>G | upstream_gene_variant | 1.0 |
| rpoC | 762392 | c.-978G>C | upstream_gene_variant | 1.0 |
| rpoC | 762395 | c.-975G>T | upstream_gene_variant | 1.0 |
| rpoC | 762398 | c.-972T>C | upstream_gene_variant | 1.0 |
| rpoC | 762404 | c.-966T>C | upstream_gene_variant | 1.0 |
| rpoC | 762410 | c.-960T>G | upstream_gene_variant | 1.0 |
| rpoC | 762416 | c.-954A>G | upstream_gene_variant | 1.0 |
| rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
| rpoC | 763034 | c.-336C>G | upstream_gene_variant | 1.0 |
| rpoC | 763040 | c.-330C>G | upstream_gene_variant | 1.0 |
| rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
| rpoC | 763082 | c.-288C>T | upstream_gene_variant | 1.0 |
| rpoC | 763088 | c.-282C>G | upstream_gene_variant | 1.0 |
| rpoC | 763094 | c.-276G>C | upstream_gene_variant | 1.0 |
| rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
| rpoC | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
| rpoC | 763136 | c.-234C>T | upstream_gene_variant | 1.0 |
| rpoC | 763145 | c.-225G>A | upstream_gene_variant | 1.0 |
| rpoC | 763157 | c.-213G>T | upstream_gene_variant | 1.0 |
| rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
| rpoC | 763172 | c.-198G>C | upstream_gene_variant | 1.0 |
| rpoC | 763435 | p.Gln22His | missense_variant | 1.0 |
| rpoC | 763443 | p.Tyr25Phe | missense_variant | 1.0 |
| rpoC | 763450 | c.81G>A | synonymous_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
| rpoC | 763492 | c.123G>C | synonymous_variant | 1.0 |
| rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
| rpoC | 764593 | c.1224C>T | synonymous_variant | 1.0 |
| rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
| rpoC | 764626 | c.1257C>T | synonymous_variant | 1.0 |
| rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764668 | c.1299C>T | synonymous_variant | 1.0 |
| rpoC | 764683 | c.1314G>A | synonymous_variant | 1.0 |
| rpoC | 764692 | c.1323C>T | synonymous_variant | 1.0 |
| rpoC | 764713 | c.1344G>T | synonymous_variant | 1.0 |
| rpoC | 764716 | c.1347G>C | synonymous_variant | 1.0 |
| rpoC | 764746 | c.1377G>T | synonymous_variant | 1.0 |
| rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
| rpoC | 764758 | c.1389C>G | synonymous_variant | 1.0 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764791 | c.1422C>G | synonymous_variant | 1.0 |
| rpoC | 764803 | c.1434C>T | synonymous_variant | 1.0 |
| rpoC | 764809 | c.1440C>T | synonymous_variant | 1.0 |
| rpoC | 764810 | p.Pro481Ala | missense_variant | 1.0 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
| rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
| rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764869 | c.1500C>T | synonymous_variant | 1.0 |
| rpoC | 764875 | c.1506C>A | synonymous_variant | 1.0 |
| rpoC | 764887 | c.1518G>C | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
| rpoC | 765300 | p.Val644Ala | missense_variant | 1.0 |
| rpoC | 765305 | p.Ile646Val | missense_variant | 1.0 |
| rpoC | 765319 | c.1950A>G | synonymous_variant | 1.0 |
| rpoC | 765323 | c.1955_1957delGCC | disruptive_inframe_deletion | 1.0 |
| rpoC | 765328 | p.His653Gln | missense_variant | 1.0 |
| rpoC | 765330 | p.Ser654Asn | missense_variant | 1.0 |
| rpoC | 765334 | c.1965C>T | synonymous_variant | 1.0 |
| rpoC | 765343 | c.1974G>A | synonymous_variant | 1.0 |
| rpoC | 765352 | c.1983G>C | synonymous_variant | 1.0 |
| rpoC | 765356 | p.Met663Val | missense_variant | 1.0 |
| rpoC | 765370 | c.2001G>A | synonymous_variant | 1.0 |
| rpoC | 765379 | c.2010G>C | synonymous_variant | 1.0 |
| rpoC | 765382 | c.2013G>T | synonymous_variant | 1.0 |
| rpoC | 765383 | p.Met672Leu | missense_variant | 1.0 |
| rpoC | 765403 | c.2034G>C | synonymous_variant | 1.0 |
| rpoC | 765405 | p.Leu679His | missense_variant | 1.0 |
| rpoC | 765409 | c.2040T>G | synonymous_variant | 1.0 |
| rpoC | 765421 | c.2052C>G | synonymous_variant | 1.0 |
| rpoC | 765449 | p.Ala694Ser | missense_variant | 1.0 |
| rpoC | 765454 | c.2085C>G | synonymous_variant | 1.0 |
| rpoC | 765469 | c.2100G>C | synonymous_variant | 1.0 |
| rpoC | 765478 | c.2109T>G | synonymous_variant | 1.0 |
| rpoC | 765480 | p.Tyr704Phe | missense_variant | 1.0 |
| rpoC | 765499 | c.2130C>G | synonymous_variant | 1.0 |
| rpoC | 765907 | c.2538G>T | synonymous_variant | 1.0 |
| rpoC | 765910 | c.2541G>C | synonymous_variant | 1.0 |
| rpoC | 765928 | c.2559C>G | synonymous_variant | 1.0 |
| rpoC | 765940 | c.2571A>T | synonymous_variant | 1.0 |
| rpoC | 765947 | c.2578T>C | synonymous_variant | 1.0 |
| rpoC | 765962 | c.2593_2595delTTGinsCTT | synonymous_variant | 1.0 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
| rpoC | 765973 | c.2604C>G | synonymous_variant | 1.0 |
| rpoC | 765979 | c.2610C>G | synonymous_variant | 1.0 |
| rpoC | 765982 | c.2613C>T | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 766003 | c.2634G>C | synonymous_variant | 1.0 |
| rpoC | 767080 | c.3711G>C | synonymous_variant | 1.0 |
| rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
| rpoC | 767104 | c.3735C>G | synonymous_variant | 1.0 |
| rpoC | 767107 | c.3738C>T | synonymous_variant | 1.0 |
| rpoC | 767119 | c.3750A>G | synonymous_variant | 1.0 |
| rpoC | 767125 | c.3756G>C | synonymous_variant | 1.0 |
| rpoC | 767134 | c.3765C>T | synonymous_variant | 1.0 |
| rpoC | 767138 | c.3769C>T | synonymous_variant | 1.0 |
| rpoC | 767149 | c.3780C>T | synonymous_variant | 1.0 |
| rpoC | 767158 | c.3789T>C | synonymous_variant | 1.0 |
| rpoC | 767180 | p.Ala1271Ser | missense_variant | 1.0 |
| rpoC | 767191 | c.3822C>G | synonymous_variant | 1.0 |
| rpoC | 767197 | c.3828G>A | synonymous_variant | 1.0 |
| rpoC | 767203 | c.3834C>G | synonymous_variant | 1.0 |
| rpoC | 767206 | c.3837C>G | synonymous_variant | 1.0 |
| rpoC | 767209 | c.3840T>C | synonymous_variant | 1.0 |
| rpoC | 767212 | c.3843G>C | synonymous_variant | 1.0 |
| rpoC | 767221 | c.3852C>G | synonymous_variant | 1.0 |
| rpoC | 767230 | c.3861G>C | synonymous_variant | 1.0 |
| rpoC | 767233 | c.3864T>C | synonymous_variant | 1.0 |
| rpsL | 781706 | c.147T>C | synonymous_variant | 1.0 |
| rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
| rpsL | 781814 | c.255C>T | synonymous_variant | 1.0 |
| rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
| rpsL | 781829 | c.270G>C | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
| rpsL | 781859 | c.300T>C | synonymous_variant | 1.0 |
| rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
| rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
| rpsL | 781877 | c.318T>A | synonymous_variant | 1.0 |
| rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>T | synonymous_variant | 1.0 |
| rpsL | 781907 | c.348T>C | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
| rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
| rplC | 800856 | c.48A>G | synonymous_variant | 1.0 |
| rplC | 800865 | p.Glu19Asp | missense_variant | 1.0 |
| rplC | 800867 | p.Ser20Asn | missense_variant | 1.0 |
| fbiC | 1304613 | c.1683T>C | synonymous_variant | 1.0 |
| fbiC | 1304634 | c.1704C>G | synonymous_variant | 1.0 |
| atpE | 1461197 | c.153A>C | synonymous_variant | 1.0 |
| rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472031 | n.186G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472032 | n.187G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472041 | n.196C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472043 | n.198T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472050 | n.205G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.86 |
| rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472846 | n.1001C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472847 | n.1002G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472848 | n.1003T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472860 | n.1015C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472861 | n.1016G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473082 | n.1237G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473288 | n.1443C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473684 | n.27G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473699 | n.43delG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473707 | n.50T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473812 | n.155G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473814 | n.157A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473839 | n.182G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473888 | n.231T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473924 | n.267_268insT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473946 | n.289A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473950 | n.293G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474061 | n.404T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474074 | n.417C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474089 | n.432C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474093 | n.436G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474100 | n.443C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474103 | n.446A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474106 | n.449_450insCT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474109 | n.453_454delAT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474181 | n.524_525insT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474184 | n.527C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474185 | n.529delA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474291 | n.635_649delTTCCTCTCCGGAGGA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474743 | n.1086T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475573 | n.1916G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475760 | n.2105_2106delGC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476085 | n.2428G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476114 | n.2457T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
| rpsA | 1833709 | c.168C>T | synonymous_variant | 1.0 |
| rpsA | 1833724 | c.183C>T | synonymous_variant | 1.0 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
| rpsA | 1833733 | c.192C>G | synonymous_variant | 1.0 |
| rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833745 | c.204G>C | synonymous_variant | 1.0 |
| rpsA | 1833748 | c.207C>G | synonymous_variant | 1.0 |
| rpsA | 1833760 | c.219C>T | synonymous_variant | 1.0 |
| rpsA | 1833787 | c.246C>G | synonymous_variant | 1.0 |
| rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
| rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>T | synonymous_variant | 1.0 |
| rpsA | 1833823 | c.282G>A | synonymous_variant | 1.0 |
| rpsA | 1833832 | c.291G>A | synonymous_variant | 1.0 |
| rpsA | 1833835 | c.294C>T | synonymous_variant | 1.0 |
| rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
| rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
| rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
| rpsA | 1833862 | c.321G>T | synonymous_variant | 1.0 |
| rpsA | 1833874 | c.333T>G | synonymous_variant | 1.0 |
| rpsA | 1833877 | c.336C>G | synonymous_variant | 1.0 |
| rpsA | 1833886 | c.345C>G | synonymous_variant | 1.0 |
| rpsA | 1833894 | p.Ala118Glu | missense_variant | 1.0 |
| rpsA | 1833961 | c.420C>G | synonymous_variant | 1.0 |
| rpsA | 1833970 | c.429G>T | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1833991 | c.450C>G | synonymous_variant | 1.0 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834009 | c.468C>T | synonymous_variant | 1.0 |
| rpsA | 1834012 | c.471G>C | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
| rpsA | 1834021 | c.480C>T | synonymous_variant | 1.0 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1834073 | p.Lys178Arg | missense_variant | 1.0 |
| rpsA | 1834096 | c.555G>C | synonymous_variant | 1.0 |
| rpsA | 1834099 | c.558C>G | synonymous_variant | 1.0 |
| rpsA | 1834108 | c.567C>G | synonymous_variant | 1.0 |
| rpsA | 1834228 | c.687C>A | synonymous_variant | 1.0 |
| rpsA | 1834231 | c.690T>G | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>T | synonymous_variant | 1.0 |
| rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
| rpsA | 1834246 | c.705G>T | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
| rpsA | 1834252 | c.711C>G | synonymous_variant | 1.0 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
| rpsA | 1834279 | c.738C>T | synonymous_variant | 1.0 |
| rpsA | 1834294 | c.753G>T | synonymous_variant | 1.0 |
| rpsA | 1834297 | c.756C>T | synonymous_variant | 1.0 |
| rpsA | 1834303 | c.762T>G | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834327 | c.786G>T | synonymous_variant | 1.0 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
| rpsA | 1834357 | c.816T>C | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834375 | c.834G>C | synonymous_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834700 | p.Gln387Ala | missense_variant | 1.0 |
| rpsA | 1834705 | c.1164C>G | synonymous_variant | 1.0 |
| rpsA | 1834720 | c.1179C>G | synonymous_variant | 1.0 |
| rpsA | 1834732 | c.1191T>C | synonymous_variant | 1.0 |
| rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
| rpsA | 1834747 | c.1206A>G | synonymous_variant | 1.0 |
| rpsA | 1834759 | c.1218A>C | synonymous_variant | 1.0 |
| rpsA | 1834765 | p.Glu408Asp | missense_variant | 1.0 |
| rpsA | 1834774 | c.1233C>T | synonymous_variant | 1.0 |
| rpsA | 1834776 | p.Ala412Glu | missense_variant | 1.0 |
| rpsA | 1834780 | c.1239A>G | synonymous_variant | 1.0 |
| rpsA | 1834789 | c.1248T>C | synonymous_variant | 1.0 |
| rpsA | 1834813 | c.1272G>T | synonymous_variant | 1.0 |
| kasA | 2517917 | c.-198G>C | upstream_gene_variant | 1.0 |
| kasA | 2517941 | c.-174C>G | upstream_gene_variant | 1.0 |
| kasA | 2517953 | c.-162C>T | upstream_gene_variant | 1.0 |
| kasA | 2517959 | c.-156C>T | upstream_gene_variant | 1.0 |
| kasA | 2517962 | c.-153C>G | upstream_gene_variant | 1.0 |
| rpoA | 3877571 | p.Pro313Thr | missense_variant | 1.0 |
| rpoA | 3877587 | c.921A>G | synonymous_variant | 1.0 |
| rpoA | 3877593 | c.915C>T | synonymous_variant | 1.0 |
| rpoA | 3877614 | c.894G>A | synonymous_variant | 1.0 |
| rpoA | 3877620 | c.888G>A | synonymous_variant | 1.0 |
| rpoA | 3877638 | c.870T>C | synonymous_variant | 1.0 |
| rpoA | 3877656 | c.852T>G | synonymous_variant | 1.0 |
| rpoA | 3877665 | c.843C>G | synonymous_variant | 1.0 |
| rpoA | 3877677 | c.831G>C | synonymous_variant | 1.0 |
| rpoA | 3877680 | c.828G>C | synonymous_variant | 1.0 |
| rpoA | 3877686 | c.822A>G | synonymous_variant | 1.0 |
| rpoA | 3877692 | c.816G>C | synonymous_variant | 1.0 |
| rpoA | 3877704 | c.804G>T | synonymous_variant | 1.0 |
| clpC1 | 4038737 | c.1968C>T | synonymous_variant | 0.75 |
| clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.75 |
| clpC1 | 4038749 | c.1956C>A | synonymous_variant | 1.0 |
| clpC1 | 4038755 | c.1950G>C | synonymous_variant | 1.0 |
| clpC1 | 4038758 | c.1947C>T | synonymous_variant | 1.0 |
| clpC1 | 4038767 | c.1938G>T | synonymous_variant | 1.0 |
| clpC1 | 4038770 | c.1935C>T | synonymous_variant | 1.0 |
| clpC1 | 4038773 | c.1932T>C | synonymous_variant | 1.0 |
| clpC1 | 4038782 | c.1923G>T | synonymous_variant | 1.0 |
| clpC1 | 4038790 | c.1915C>T | synonymous_variant | 1.0 |
| clpC1 | 4038795 | p.Ser637Thr | missense_variant | 1.0 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
| clpC1 | 4038815 | c.1890G>T | synonymous_variant | 1.0 |
| clpC1 | 4038842 | c.1863G>C | synonymous_variant | 1.0 |
| clpC1 | 4038845 | c.1858_1860delTCGinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4038860 | c.1845G>T | synonymous_variant | 1.0 |
| clpC1 | 4038989 | c.1716T>C | synonymous_variant | 1.0 |
| clpC1 | 4038997 | c.1708T>C | synonymous_variant | 1.0 |
| clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
| clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
| clpC1 | 4039178 | c.1527G>C | synonymous_variant | 1.0 |
| clpC1 | 4039183 | c.1522T>C | synonymous_variant | 1.0 |
| clpC1 | 4039190 | c.1515C>T | synonymous_variant | 1.0 |
| clpC1 | 4039196 | c.1509G>A | synonymous_variant | 1.0 |
| clpC1 | 4039199 | p.Ala502Glu | missense_variant | 1.0 |
| clpC1 | 4039208 | c.1497C>G | synonymous_variant | 1.0 |
| clpC1 | 4039220 | c.1485G>C | synonymous_variant | 1.0 |
| clpC1 | 4039262 | c.1443C>T | synonymous_variant | 1.0 |
| clpC1 | 4039265 | c.1440C>T | synonymous_variant | 1.0 |
| clpC1 | 4039271 | c.1434G>A | synonymous_variant | 1.0 |
| clpC1 | 4039283 | c.1422C>T | synonymous_variant | 1.0 |
| clpC1 | 4039286 | c.1417_1419delCTTinsTTA | synonymous_variant | 1.0 |
| clpC1 | 4039289 | c.1416T>C | synonymous_variant | 1.0 |
| clpC1 | 4039292 | c.1413C>T | synonymous_variant | 1.0 |
| clpC1 | 4039304 | c.1401G>A | synonymous_variant | 1.0 |
| clpC1 | 4039316 | p.Glu463Asp | missense_variant | 1.0 |
| clpC1 | 4039319 | c.1386T>C | synonymous_variant | 1.0 |
| clpC1 | 4039328 | c.1377A>G | synonymous_variant | 1.0 |
| clpC1 | 4039331 | c.1374C>G | synonymous_variant | 1.0 |
| clpC1 | 4039337 | p.Thr456Gln | missense_variant | 1.0 |
| clpC1 | 4039347 | p.Arg453Ser | missense_variant | 1.0 |
| clpC1 | 4039360 | p.Ser449Arg | missense_variant | 1.0 |
| clpC1 | 4039361 | c.1344C>G | synonymous_variant | 1.0 |
| clpC1 | 4039454 | c.1251A>T | synonymous_variant | 1.0 |
| clpC1 | 4039466 | c.1239T>C | synonymous_variant | 1.0 |
| clpC1 | 4039469 | c.1236T>C | synonymous_variant | 1.0 |
| clpC1 | 4039472 | c.1233G>C | synonymous_variant | 1.0 |
| clpC1 | 4039478 | c.1227G>C | synonymous_variant | 1.0 |
| clpC1 | 4039481 | c.1224T>C | synonymous_variant | 1.0 |
| clpC1 | 4039487 | c.1218G>C | synonymous_variant | 1.0 |
| clpC1 | 4039522 | c.1183C>T | synonymous_variant | 1.0 |
| clpC1 | 4039528 | c.1177C>A | synonymous_variant | 1.0 |
| clpC1 | 4039541 | c.1164C>G | synonymous_variant | 1.0 |
| clpC1 | 4039544 | c.1161C>T | synonymous_variant | 1.0 |
| clpC1 | 4039556 | c.1149G>C | synonymous_variant | 1.0 |
| clpC1 | 4039559 | c.1146C>G | synonymous_variant | 1.0 |
| clpC1 | 4039565 | c.1140G>T | synonymous_variant | 1.0 |
| clpC1 | 4039570 | p.Met379Leu | missense_variant | 1.0 |
| clpC1 | 4039574 | p.Ala377Gly | missense_variant | 1.0 |
| clpC1 | 4039586 | c.1119G>C | synonymous_variant | 1.0 |
| clpC1 | 4039610 | c.1095G>C | synonymous_variant | 1.0 |
| clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
| clpC1 | 4039622 | c.1083C>T | synonymous_variant | 1.0 |
| clpC1 | 4039649 | c.1056G>C | synonymous_variant | 1.0 |
| clpC1 | 4039661 | c.1044T>C | synonymous_variant | 1.0 |
| clpC1 | 4039682 | c.1023C>G | synonymous_variant | 1.0 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039733 | c.972G>T | synonymous_variant | 1.0 |
| clpC1 | 4039739 | c.966C>G | synonymous_variant | 1.0 |
| clpC1 | 4039742 | c.963C>T | synonymous_variant | 1.0 |
| clpC1 | 4039748 | c.957G>C | synonymous_variant | 1.0 |
| clpC1 | 4039751 | c.954A>G | synonymous_variant | 1.0 |
| clpC1 | 4039757 | c.948A>G | synonymous_variant | 1.0 |
| clpC1 | 4039760 | c.945T>C | synonymous_variant | 1.0 |
| clpC1 | 4039763 | c.942C>T | synonymous_variant | 1.0 |
| clpC1 | 4039769 | c.936C>G | synonymous_variant | 1.0 |
| clpC1 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
| clpC1 | 4039793 | c.912C>G | synonymous_variant | 1.0 |
| clpC1 | 4039814 | c.891C>G | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>C | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>G | synonymous_variant | 1.0 |
| clpC1 | 4039826 | c.879C>G | synonymous_variant | 1.0 |
| clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
| clpC1 | 4039832 | c.873C>G | synonymous_variant | 1.0 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
| clpC1 | 4039868 | c.837C>T | synonymous_variant | 1.0 |
| clpC1 | 4039913 | c.792C>T | synonymous_variant | 1.0 |
| clpC1 | 4039931 | c.774T>C | synonymous_variant | 1.0 |
| clpC1 | 4039934 | c.771G>C | synonymous_variant | 1.0 |
| clpC1 | 4040048 | c.657C>T | synonymous_variant | 1.0 |
| clpC1 | 4040087 | c.618G>C | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4040093 | c.612C>G | synonymous_variant | 1.0 |
| clpC1 | 4040126 | c.579C>T | synonymous_variant | 1.0 |
| clpC1 | 4040141 | c.564C>T | synonymous_variant | 1.0 |
| clpC1 | 4040144 | c.561G>C | synonymous_variant | 1.0 |
| clpC1 | 4040147 | c.558A>G | synonymous_variant | 1.0 |
| clpC1 | 4040153 | c.552A>G | synonymous_variant | 1.0 |
| clpC1 | 4040159 | c.546G>C | synonymous_variant | 1.0 |
| clpC1 | 4040387 | c.318A>G | synonymous_variant | 1.0 |
| clpC1 | 4040393 | c.312G>C | synonymous_variant | 1.0 |
| clpC1 | 4040411 | c.294T>C | synonymous_variant | 1.0 |
| clpC1 | 4040423 | c.282A>G | synonymous_variant | 1.0 |
| clpC1 | 4040426 | c.279T>C | synonymous_variant | 1.0 |
| clpC1 | 4040431 | c.274T>C | synonymous_variant | 1.0 |
| clpC1 | 4040441 | c.264C>G | synonymous_variant | 1.0 |
| clpC1 | 4040444 | c.261C>G | synonymous_variant | 1.0 |
| clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
| clpC1 | 4040456 | c.249C>T | synonymous_variant | 1.0 |
| clpC1 | 4040459 | c.246C>G | synonymous_variant | 1.0 |
| clpC1 | 4040462 | c.243C>T | synonymous_variant | 1.0 |
| clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
| clpC1 | 4040480 | c.225T>C | synonymous_variant | 1.0 |
| clpC1 | 4040495 | c.210C>T | synonymous_variant | 1.0 |
| clpC1 | 4040522 | c.183T>C | synonymous_variant | 1.0 |
| clpC1 | 4040531 | c.174T>G | synonymous_variant | 1.0 |
| clpC1 | 4040540 | c.165G>T | synonymous_variant | 1.0 |
| clpC1 | 4040546 | c.159G>C | synonymous_variant | 1.0 |
| clpC1 | 4040558 | c.147G>C | synonymous_variant | 1.0 |
| clpC1 | 4040561 | c.144A>G | synonymous_variant | 1.0 |
| clpC1 | 4040579 | c.126A>G | synonymous_variant | 1.0 |
| clpC1 | 4040582 | c.123G>C | synonymous_variant | 1.0 |
| clpC1 | 4040585 | c.120A>G | synonymous_variant | 1.0 |
| clpC1 | 4040597 | c.108C>T | synonymous_variant | 1.0 |
| clpC1 | 4040600 | c.103_105delTTAinsCTG | synonymous_variant | 1.0 |
| clpC1 | 4040603 | c.102T>G | synonymous_variant | 1.0 |
| clpC1 | 4040606 | c.99T>C | synonymous_variant | 1.0 |
| embC | 4241104 | c.1242G>A | synonymous_variant | 1.0 |
| embC | 4241108 | p.Ala416Ser | missense_variant | 1.0 |
| embC | 4241111 | p.Val417Ile | missense_variant | 1.0 |
| embC | 4241121 | p.Ser420Asn | missense_variant | 1.0 |
| embC | 4241134 | c.1272G>T | synonymous_variant | 1.0 |
| embC | 4241136 | p.Val425Ala | missense_variant | 1.0 |
| embC | 4241140 | c.1278A>C | synonymous_variant | 1.0 |
| embC | 4241141 | p.Ile427Ala | missense_variant | 1.0 |
| embC | 4241158 | c.1296T>C | synonymous_variant | 1.0 |
| embC | 4241161 | c.1299C>G | synonymous_variant | 1.0 |
| embC | 4241162 | c.1300_1302delTTGinsCTC | synonymous_variant | 1.0 |
| embC | 4241168 | c.1306C>T | synonymous_variant | 1.0 |
| embC | 4241179 | c.1317G>C | synonymous_variant | 1.0 |
| embC | 4241182 | c.1320G>C | synonymous_variant | 1.0 |
| embC | 4241185 | c.1323G>C | synonymous_variant | 1.0 |
| embC | 4241188 | c.1326C>T | synonymous_variant | 1.0 |
| embC | 4241194 | c.1332C>G | synonymous_variant | 1.0 |
| embC | 4241197 | c.1335G>C | synonymous_variant | 1.0 |
| embC | 4241203 | c.1341T>C | synonymous_variant | 1.0 |
