CHR | GENE | LOCUS | PRODUCT | TYPE | EFFECT | POS | REF | ALT | BIOTYPE | NUCLEOTIDE | CONSEQUENCE | IMPACT | PATHWAY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Chromosome | Rv3753c | Rv3753c | O69720 | snp | missense_variant | 4200220 | G | A | protein_coding | c.2C>T | p.Thr1Met | MODERATE |
NA |
Chromosome | Rv3756c | Rv3756c | O69722 | snp | synonymous_variant | 4202383 | C | A | protein_coding | c.231G>T | p.Val77Val | LOW | |
Chromosome | Rv3759c | Rv3759c | O69725 | snp | missense_variant | 4205120 | G | A | protein_coding | c.254C>T | p.Pro85Leu | MODERATE | |
Chromosome | Rv3764c | Rv3764c | O69729 | snp | missense_variant | 4210876 | C | T | protein_coding | c.134G>A | p.Arg45His | MODERATE |
NA |
Chromosome | Rv3769 | Rv3769 | P72036 | snp | missense_variant | 4214747 | C | T | protein_coding | c.133C>T | p.His45Tyr | MODERATE |
NA |
Chromosome | Rv3770c | Rv3770c | P72037 | snp | missense_variant | 4215484 | C | G | protein_coding | c.292G>C | p.Ala98Pro | MODERATE |
NA |
Chromosome | Rv3772 | Rv3772 | P9WML5 | snp | missense_variant | 4217557 | G | A | protein_coding | c.424G>A | p.Ala142Thr | MODERATE | |
Chromosome | Rv3777 | Rv3777 | P72043 | snp | missense_variant | 4223172 | C | T | protein_coding | c.479C>T | p.Ala160Val | MODERATE |
NA |
Chromosome | Rv3785 | Rv3785 | P9WKX1 | snp | synonymous_variant | 4232327 | G | A | protein_coding | c.1008G>A | p.Arg336Arg | LOW |
NA |
Chromosome | Rv3792 | Rv3792 | P9WN03 | snp | synonymous_variant | 4238963 | C | T | protein_coding | c.1032C>T | p.His344His | LOW | |
Chromosome | Rv3792 | Rv3792 | P9WN03 | snp | missense_variant | 4239274 | C | G | protein_coding | c.1343C>G | p.Pro448Arg | MODERATE | |
Chromosome | Rv3793 | Rv3793 | P9WNL5 | snp | missense_variant | 4240671 | T | C | protein_coding | c.809T>C | p.Ile270Thr | MODERATE | |
Chromosome | Rv3795 | Rv3795 | P9WNL7 | snp | missense_variant | 4247429 | A | G | protein_coding | c.916A>G | p.Met306Val | MODERATE | |
Chromosome | Rv3795 | Rv3795 | P9WNL7 | snp | missense_variant | 4247646 | C | A | protein_coding | c.1133C>A | p.Ala378Glu | MODERATE | |
Chromosome | Rv3797 | Rv3797 | O53577 | snp | synonymous_variant | 4251297 | C | G | protein_coding | c.213C>G | p.Gly71Gly | LOW |
NA |
Chromosome | Rv3798 | Rv3798 |
NA |
snp | missense_variant | 4254290 | T | G | protein_coding | c.1298T>G | p.Leu433Arg | MODERATE |
NA |
Chromosome | Rv3799c | Rv3799c | O53578 | snp | missense_variant | 4254478 | G | A | protein_coding | c.1471C>T | p.His491Tyr | MODERATE |
NA |
Chromosome | Rv3801c | Rv3801c | O53580 | snp | missense_variant | 4261499 | A | G | protein_coding | c.1568T>C | p.Val523Ala | MODERATE |
NA |
CHR | GENE | LOCUS | PRODUCT | TYPE | EFFECT | POS | REF | ALT | BIOTYPE | NUCLEOTIDE | CONSEQUENCE | IMPACT | PATHWAY |