Run ID: SRR3675537
Sample name:
Date: 04-04-2023 05:32:31
Number of reads: 15774
Percentage reads mapped: 4.09
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 | 6982 | c.-320A>G | upstream_gene_variant | 1.0 |
gyrA | 6985 | c.-317C>T | upstream_gene_variant | 1.0 |
gyrA | 6988 | c.-314C>G | upstream_gene_variant | 1.0 |
gyrA | 7006 | c.-296T>G | upstream_gene_variant | 1.0 |
gyrB | 7010 | p.Leu591Met | missense_variant | 1.0 |
gyrA | 7015 | c.-287G>A | upstream_gene_variant | 1.0 |
gyrA | 7018 | c.-284G>C | upstream_gene_variant | 1.0 |
gyrA | 7024 | c.-278G>C | upstream_gene_variant | 1.0 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 1.0 |
gyrB | 7051 | p.Glu604Asp | missense_variant | 1.0 |
gyrA | 7060 | c.-242T>C | upstream_gene_variant | 1.0 |
gyrA | 7066 | c.-236G>T | upstream_gene_variant | 1.0 |
gyrA | 7078 | c.-224A>G | 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 |
gyrA | 7745 | c.444G>A | synonymous_variant | 1.0 |
gyrA | 7760 | c.459C>T | synonymous_variant | 1.0 |
gyrA | 7763 | c.462T>G | synonymous_variant | 1.0 |
rpoB | 760481 | c.675G>C | 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 | 760561 | c.757_758delCG | frameshift_variant | 1.0 |
rpoB | 760567 | p.Ser254Trp | missense_variant | 1.0 |
rpoB | 760568 | c.762_763insGC | frameshift_variant | 1.0 |
rpoB | 760571 | c.765G>C | synonymous_variant | 1.0 |
rpoB | 760588 | p.Thr261Ile | missense_variant | 1.0 |
rpoB | 760591 | p.Val262Ala | missense_variant | 1.0 |
rpoB | 760595 | c.789C>T | synonymous_variant | 1.0 |
rpoB | 760596 | p.Thr264Pro | missense_variant | 1.0 |
rpoB | 760608 | c.802C>T | synonymous_variant | 1.0 |
rpoB | 760611 | c.805T>C | synonymous_variant | 1.0 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 1.0 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 1.0 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 1.0 |
rpoB | 760841 | c.1035T>C | synonymous_variant | 1.0 |
rpoB | 760858 | p.Val351Ala | missense_variant | 1.0 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 1.0 |
rpoB | 760865 | c.1059C>T | synonymous_variant | 1.0 |
rpoB | 760886 | p.Glu360Asp | missense_variant | 1.0 |
rpoB | 760887 | p.Thr361Val | missense_variant | 1.0 |
rpoB | 760910 | c.1104C>T | synonymous_variant | 1.0 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 1.0 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 1.0 |
rpoB | 760943 | c.1137C>T | synonymous_variant | 1.0 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
rpoB | 760965 | p.Met387Leu | missense_variant | 1.0 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 1.0 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 1.0 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 1.0 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 1.0 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 1.0 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 1.0 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 1.0 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 1.0 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 1.0 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 1.0 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 1.0 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 1.0 |
rpoB | 761936 | c.2130C>T | synonymous_variant | 1.0 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 1.0 |
rpoB | 761954 | c.2148C>A | synonymous_variant | 1.0 |
rpoB | 761955 | p.Ile717Val | missense_variant | 1.0 |
rpoB | 761969 | c.2163G>A | synonymous_variant | 1.0 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.75 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.75 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.75 |
rpoB | 762038 | c.2232C>T | synonymous_variant | 0.67 |
rpoB | 762047 | c.2241G>A | synonymous_variant | 0.67 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.67 |
rpoB | 762056 | c.2250G>A | synonymous_variant | 0.67 |
rpoB | 762065 | c.2259T>G | synonymous_variant | 0.67 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.67 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 1.0 |
rpoC | 763528 | c.159G>A | synonymous_variant | 1.0 |
rpoC | 763531 | c.162G>T | synonymous_variant | 1.0 |
rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
rpoC | 763657 | c.288G>A | synonymous_variant | 1.0 |
rpoC | 763879 | c.510A>G | synonymous_variant | 1.0 |
rpoC | 763888 | c.519G>T | synonymous_variant | 1.0 |
rpoC | 763891 | c.522G>C | synonymous_variant | 1.0 |
rpoC | 763894 | c.525A>G | synonymous_variant | 1.0 |
rpoC | 763900 | c.531G>C | synonymous_variant | 1.0 |
rpoC | 763933 | c.564C>T | synonymous_variant | 1.0 |
rpoC | 763940 | p.Ala191Ser | missense_variant | 1.0 |
rpoC | 763945 | c.576T>C | synonymous_variant | 1.0 |
rpoC | 763947 | p.Ala193Val | missense_variant | 1.0 |
rpoC | 763951 | c.582G>C | synonymous_variant | 1.0 |
rpoC | 763960 | c.591T>G | synonymous_variant | 1.0 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 1.0 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 1.0 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 1.0 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
rpoC | 764510 | c.1141C>T | synonymous_variant | 1.0 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 1.0 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 1.0 |
rpoC | 767008 | c.3639G>A | synonymous_variant | 1.0 |
rpoC | 767023 | c.3654C>T | synonymous_variant | 0.67 |
rpoC | 767044 | c.3675G>C | synonymous_variant | 0.67 |
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 | 767179 | c.3810C>T | 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 |
rpsL | 781706 | c.147T>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 | 1471956 | n.111A>C | non_coding_transcript_exon_variant | 0.33 |
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 | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472287 | n.442C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472327 | n.482G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472337 | n.492C>G | 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 | 1.0 |
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 | 0.85 |
rrs | 1472847 | n.1002G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472848 | n.1003T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472860 | n.1015C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472861 | n.1016G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.95 |
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 | 1473770 | n.113T>C | 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 | 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 | 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 | 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 | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474413 | n.756A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474415 | n.759_781delCACACGCGCATACGCGCGTGTGA | 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 | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474507 | n.850G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474639 | n.982G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474640 | n.983C>T | 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 | 1475061 | n.1406delA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475129 | n.1472G>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 | 0.88 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475573 | n.1916G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475760 | n.2105_2106delGC | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476030 | n.2373A>G | 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 |
rrl | 1476665 | n.3008T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476684 | n.3027C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833616 | c.75A>T | synonymous_variant | 1.0 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 1.0 |
rpsA | 1833625 | c.84A>G | synonymous_variant | 1.0 |
rpsA | 1833664 | c.123C>G | synonymous_variant | 1.0 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
rpsA | 1833679 | c.138G>T | synonymous_variant | 1.0 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 1.0 |
rpsA | 1833691 | c.150G>A | synonymous_variant | 1.0 |
rpsA | 1833697 | c.156C>T | synonymous_variant | 1.0 |
rpsA | 1833700 | c.159C>T | synonymous_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 | 1833838 | c.297G>C | synonymous_variant | 1.0 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
rpsA | 1833949 | c.408T>C | synonymous_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 | 1834033 | c.492C>T | synonymous_variant | 1.0 |
rpsA | 1834073 | p.Lys178Arg | missense_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 | 1834396 | c.855G>C | synonymous_variant | 1.0 |
rpsA | 1834411 | c.870T>G | synonymous_variant | 1.0 |
rpsA | 1834414 | c.873C>T | synonymous_variant | 1.0 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 1.0 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
rpsA | 1834429 | c.888C>T | synonymous_variant | 1.0 |
rpsA | 1834438 | c.897C>T | synonymous_variant | 1.0 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 1.0 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 1.0 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
rpsA | 1834477 | c.936C>T | synonymous_variant | 1.0 |
rpsA | 1834489 | c.948T>C | 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 | 2517962 | c.-153C>G | upstream_gene_variant | 1.0 |
kasA | 2517968 | c.-147T>A | upstream_gene_variant | 1.0 |
kasA | 2517974 | c.-141T>C | upstream_gene_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 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 1.0 |
rpoA | 3877731 | c.777G>C | synonymous_variant | 1.0 |
rpoA | 3877734 | c.774G>C | synonymous_variant | 1.0 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 1.0 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 1.0 |
rpoA | 3877749 | c.759C>T | synonymous_variant | 1.0 |
rpoA | 3877752 | p.Asp252Glu | missense_variant | 1.0 |
rpoA | 3877755 | c.753C>T | synonymous_variant | 1.0 |
rpoA | 3877758 | c.750G>C | synonymous_variant | 1.0 |
rpoA | 3877764 | c.744C>A | synonymous_variant | 1.0 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 1.0 |
rpoA | 3877773 | c.735G>C | synonymous_variant | 1.0 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 1.0 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 1.0 |
rpoA | 3877797 | c.711G>A | synonymous_variant | 1.0 |
rpoA | 3877815 | c.693C>T | synonymous_variant | 1.0 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 1.0 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 1.0 |
rpoA | 3877839 | c.669G>A | synonymous_variant | 1.0 |
rpoA | 3877896 | c.612G>A | synonymous_variant | 1.0 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 1.0 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 1.0 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 1.0 |
rpoA | 3877923 | c.585C>T | synonymous_variant | 1.0 |
rpoA | 3877931 | p.Ile193Val | missense_variant | 1.0 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 1.0 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 1.0 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 1.0 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 1.0 |
rpoA | 3878301 | c.207C>G | synonymous_variant | 1.0 |
rpoA | 3878310 | c.198G>T | synonymous_variant | 1.0 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 1.0 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 1.0 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 1.0 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
clpC1 | 4039046 | c.1659C>G | synonymous_variant | 1.0 |
clpC1 | 4039070 | c.1635G>C | synonymous_variant | 1.0 |
clpC1 | 4039077 | p.Lys543Arg | missense_variant | 1.0 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 1.0 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 1.0 |
clpC1 | 4039091 | c.1614G>T | synonymous_variant | 1.0 |
clpC1 | 4039097 | c.1608G>T | synonymous_variant | 1.0 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 1.0 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 1.0 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.86 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.83 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.75 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.75 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.8 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.8 |
clpC1 | 4039190 | c.1515C>T | synonymous_variant | 0.8 |
clpC1 | 4039196 | c.1509G>A | synonymous_variant | 0.8 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.75 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.8 |
clpC1 | 4039220 | c.1485G>C | synonymous_variant | 0.8 |
clpC1 | 4039262 | c.1443C>T | synonymous_variant | 1.0 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.67 |
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 | 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 | 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 | 4039571 | c.1134G>A | synonymous_variant | 1.0 |
clpC1 | 4039574 | p.Ala377Gly | missense_variant | 1.0 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 1.0 |
clpC1 | 4039601 | c.1104G>A | synonymous_variant | 1.0 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 1.0 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
clpC1 | 4039619 | c.1086G>A | 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 | 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 | 0.83 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.83 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 0.8 |
clpC1 | 4039946 | c.759A>G | synonymous_variant | 0.8 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.8 |
clpC1 | 4039957 | c.748C>T | synonymous_variant | 0.8 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.8 |
clpC1 | 4039964 | c.741C>G | synonymous_variant | 0.8 |
clpC1 | 4039975 | p.Asp244Asn | missense_variant | 0.8 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.8 |
clpC1 | 4039982 | c.723G>A | synonymous_variant | 0.8 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.67 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.75 |
clpC1 | 4040021 | c.684A>T | synonymous_variant | 0.67 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.67 |
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 | 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 |