Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.148741786T>A | CA354888938 | AGTR1 | c.751T>A (p.Phe251Ile) c.838T>A (p.Phe280Ile) c.856T>A (p.Phe286Ile) | |
3 | g.148741786T>C | CA354888935 | AGTR1 | c.751T>C (p.Phe251Leu) c.838T>C (p.Phe280Leu) c.856T>C (p.Phe286Leu) | |
3 | g.148741786T>G | CA354888937 | AGTR1 | c.751T>G (p.Phe251Val) c.838T>G (p.Phe280Val) c.856T>G (p.Phe286Val) | |
3 | g.148741787T>A | CA354888940 | AGTR1 | c.752T>A (p.Phe251Tyr) c.839T>A (p.Phe280Tyr) c.857T>A (p.Phe286Tyr) | |
3 | g.148741787T>C | CA354888942 | AGTR1 | c.752T>C (p.Phe251Ser) c.839T>C (p.Phe280Ser) c.857T>C (p.Phe286Ser) | |
3 | g.148741787T>G | CA354888943 | AGTR1 | c.752T>G (p.Phe251Cys) c.839T>G (p.Phe280Cys) c.857T>G (p.Phe286Cys) | |
3 | g.148741788T>A | CA354888944 | AGTR1 | c.753T>A (p.Phe251Leu) c.840T>A (p.Phe280Leu) c.858T>A (p.Phe286Leu) | COSMIC |
3 | g.148741788T>C | CA436389588 | AGTR1 | c.753T>C (p.Phe251=) c.840T>C (p.Phe280=) c.858T>C (p.Phe286=) | |
3 | g.148741788T>G | CA354888945 | AGTR1 | c.753T>G (p.Phe251Leu) c.840T>G (p.Phe280Leu) c.858T>G (p.Phe286Leu) | |
3 | g.148741789T>A | CA354888950 | AGTR1 | c.754T>A (p.Ser252Thr) c.841T>A (p.Ser281Thr) c.859T>A (p.Ser287Thr) | |
3 | g.148741789T>C | CA354888956 | AGTR1 | c.754T>C (p.Ser252Pro) c.841T>C (p.Ser281Pro) c.859T>C (p.Ser287Pro) | |
3 | g.148741789T>G | CA354888952 | AGTR1 | c.754T>G (p.Ser252Ala) c.841T>G (p.Ser281Ala) c.859T>G (p.Ser287Ala) | |
3 | g.148741790C>A | CA354888960 | AGTR1 | c.755C>A (p.Ser252Tyr) c.842C>A (p.Ser281Tyr) c.860C>A (p.Ser287Tyr) | |
3 | g.148741790C= | CA1409910164 | AGTR1 | c.755C= (p.Ser252=) c.842C= (p.Ser281=) c.860C= (p.Ser287=) | |
3 | g.148741790C>G | CA354888961 | AGTR1 | c.755C>G (p.Ser252Cys) c.842C>G (p.Ser281Cys) c.860C>G (p.Ser287Cys) | |
3 | g.148741790C>T | CA354888964 | AGTR1 | c.755C>T (p.Ser252Phe) c.842C>T (p.Ser281Phe) c.860C>T (p.Ser287Phe) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.148741791C>A | CA436389589 | AGTR1 | c.756C>A (p.Ser252=) c.843C>A (p.Ser281=) c.861C>A (p.Ser287=) | |
3 | g.148741791C>G | CA436389590 | AGTR1 | c.756C>G (p.Ser252=) c.843C>G (p.Ser281=) c.861C>G (p.Ser287=) | |
3 | g.148741791C>T | CA436389592 | AGTR1 | c.756C>T (p.Ser252=) c.843C>T (p.Ser281=) c.861C>T (p.Ser287=) | |
3 | g.148741792T>A | CA354888969 | AGTR1 | c.757T>A (p.Trp253Arg) c.844T>A (p.Trp282Arg) c.862T>A (p.Trp288Arg) | gnomAD v4 |
3 | g.148741792T>C | CA354888971 | AGTR1 | c.757T>C (p.Trp253Arg) c.844T>C (p.Trp282Arg) c.862T>C (p.Trp288Arg) | |
3 | g.148741792T>G | CA354888977 | AGTR1 | c.757T>G (p.Trp253Gly) c.844T>G (p.Trp282Gly) c.862T>G (p.Trp288Gly) | |
3 | g.148741793G>A | CA354888982 | AGTR1 | c.758G>A (p.Trp253Ter) c.845G>A (p.Trp282Ter) c.863G>A (p.Trp288Ter) | |
3 | g.148741793G>C | CA354888983 | AGTR1 | c.758G>C (p.Trp253Ser) c.845G>C (p.Trp282Ser) c.863G>C (p.Trp288Ser) | |
3 | g.148741793G>T | CA354888984 | AGTR1 | c.758G>T (p.Trp253Leu) c.845G>T (p.Trp282Leu) c.863G>T (p.Trp288Leu) | |
3 | g.148741794G>A | CA354888985 | AGTR1 | c.759G>A (p.Trp253Ter) c.846G>A (p.Trp282Ter) c.864G>A (p.Trp288Ter) | COSMIC |
3 | g.148741794G>C | CA354888986 | AGTR1 | c.759G>C (p.Trp253Cys) c.846G>C (p.Trp282Cys) c.864G>C (p.Trp288Cys) | |
3 | g.148741794G>T | CA354888988 | AGTR1 | c.759G>T (p.Trp253Cys) c.846G>T (p.Trp282Cys) c.864G>T (p.Trp288Cys) | |
3 | g.148741795A>C | CA354888991 | AGTR1 | c.760A>C (p.Ile254Leu) c.847A>C (p.Ile283Leu) c.865A>C (p.Ile289Leu) | |
3 | g.148741795A>G | CA354888995 | AGTR1 | c.760A>G (p.Ile254Val) c.847A>G (p.Ile283Val) c.865A>G (p.Ile289Val) | |
3 | g.148741795A>T | CA354888989 | AGTR1 | c.760A>T (p.Ile254Phe) c.847A>T (p.Ile283Phe) c.865A>T (p.Ile289Phe) | |
3 | g.148741796T>A | CA354889000 | AGTR1 | c.761T>A (p.Ile254Asn) c.848T>A (p.Ile283Asn) c.866T>A (p.Ile289Asn) | ClinVar dbSNP |
3 | g.148741796T>C | CA354888998 | AGTR1 | c.761T>C (p.Ile254Thr) c.848T>C (p.Ile283Thr) c.866T>C (p.Ile289Thr) | |
3 | g.148741796T>G | CA354889001 | AGTR1 | c.761T>G (p.Ile254Ser) c.848T>G (p.Ile283Ser) c.866T>G (p.Ile289Ser) | |
3 | g.148741797T>A | CA436389594 | AGTR1 | c.762T>A (p.Ile254=) c.849T>A (p.Ile283=) c.867T>A (p.Ile289=) | |
3 | g.148741797T>C | CA436389595 | AGTR1 | c.762T>C (p.Ile254=) c.849T>C (p.Ile283=) c.867T>C (p.Ile289=) | |
3 | g.148741797T>G | CA354889003 | AGTR1 | c.762T>G (p.Ile254Met) c.849T>G (p.Ile283Met) c.867T>G (p.Ile289Met) | |
3 | g.148741798C>A | CA354889014 | AGTR1 | c.763C>A (p.Pro255Thr) c.850C>A (p.Pro284Thr) c.868C>A (p.Pro290Thr) | gnomAD v4 |
3 | g.148741798C>G | CA354889006 | AGTR1 | c.763C>G (p.Pro255Ala) c.850C>G (p.Pro284Ala) c.868C>G (p.Pro290Ala) | |
3 | g.148741798C>T | CA354889008 | AGTR1 | c.763C>T (p.Pro255Ser) c.850C>T (p.Pro284Ser) c.868C>T (p.Pro290Ser) | gnomAD v4 |
3 | g.148741799C>A | CA354889016 | AGTR1 | c.764C>A (p.Pro255His) c.851C>A (p.Pro284His) c.869C>A (p.Pro290His) | |
3 | g.148741799C= | CA1409910170 | AGTR1 | c.764C= (p.Pro255=) c.851C= (p.Pro284=) c.869C= (p.Pro290=) | |
3 | g.148741799C>G | CA354889018 | AGTR1 | c.764C>G (p.Pro255Arg) c.851C>G (p.Pro284Arg) c.869C>G (p.Pro290Arg) | |
3 | g.148741799C>T | CA10617600 | AGTR1 | c.764C>T (p.Pro255Leu) c.851C>T (p.Pro284Leu) c.869C>T (p.Pro290Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
3 | g.148741800C>A | CA2657383 | AGTR1 | c.765C>A (p.Pro255=) c.852C>A (p.Pro284=) c.870C>A (p.Pro290=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.148741800C= | CA1409910176 | AGTR1 | c.765C= (p.Pro255=) c.852C= (p.Pro284=) c.870C= (p.Pro290=) | |
3 | g.148741800C>G | CA436389598 | AGTR1 | c.765C>G (p.Pro255=) c.852C>G (p.Pro284=) c.870C>G (p.Pro290=) | |
3 | g.148741800C>T | CA436389600 | AGTR1 | c.765C>T (p.Pro255=) c.852C>T (p.Pro284=) c.870C>T (p.Pro290=) | |
3 | g.148741801C>A | CA2657384 | AGTR1 | c.766C>A (p.His256Asn) c.853C>A (p.His285Asn) c.871C>A (p.His291Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
3 | g.148741801C= | CA1409910178 | AGTR1 | c.766C= (p.His256=) c.853C= (p.His285=) c.871C= (p.His291=) |