Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.154571202T>A | CA342629894 | CHRNB2 | c.379T>A (p.Tyr127Asn) c.385T>A (p.Tyr129Asn) c.-9-123T>A (n.-9-123T>A) n.631T>A | |
1 | g.154571202T>C | CA342629896 | CHRNB2 | c.379T>C (p.Tyr127His) c.385T>C (p.Tyr129His) c.-9-123T>C (n.-9-123T>C) n.631T>C | gnomAD v4 |
1 | g.154571202T>G | CA342629895 | CHRNB2 | c.379T>G (p.Tyr127Asp) c.385T>G (p.Tyr129Asp) c.-9-123T>G (n.-9-123T>G) n.631T>G | |
1 | g.154571203A>C | CA342629897 | CHRNB2 | c.380A>C (p.Tyr127Ser) c.386A>C (p.Tyr129Ser) c.-9-122A>C (n.-9-122A>C) n.632A>C | |
1 | g.154571203A>G | CA342629898 | CHRNB2 | c.380A>G (p.Tyr127Cys) c.386A>G (p.Tyr129Cys) c.-9-122A>G (n.-9-122A>G) n.632A>G | |
1 | g.154571203A>T | CA342629899 | CHRNB2 | c.380A>T (p.Tyr127Phe) c.386A>T (p.Tyr129Phe) c.-9-122A>T (n.-9-122A>T) n.632A>T | |
1 | g.154571204C>A | CA342629900 | CHRNB2 | c.381C>A (p.Tyr127Ter) c.387C>A (p.Tyr129Ter) c.-9-121C>A (n.-9-121C>A) n.633C>A | |
1 | g.154571204C= | CA1143455884 | CHRNB2 | c.381C= (p.Tyr127=) c.387C= (p.Tyr129=) c.-9-121C= (n.-9-121C=) n.633C= | |
1 | g.154571204C>G | CA342629901 | CHRNB2 | c.381C>G (p.Tyr127Ter) c.387C>G (p.Tyr129Ter) c.-9-121C>G (n.-9-121C>G) n.633C>G | |
1 | g.154571204C>T | CA30834056 | CHRNB2 | c.381C>T (p.Tyr127=) c.387C>T (p.Tyr129=) c.-9-121C>T (n.-9-121C>T) n.633C>T | dbSNP gnomAD v3 gnomAD v4 COSMIC |
1 | g.154571205G>A | CA342629902 | CHRNB2 | c.382G>A (p.Glu128Lys) c.388G>A (p.Glu130Lys) c.-9-120G>A (n.-9-120G>A) n.634G>A | gnomAD v4 COSMIC |
1 | g.154571205G>C | CA342629903 | CHRNB2 | c.382G>C (p.Glu128Gln) c.388G>C (p.Glu130Gln) c.-9-120G>C (n.-9-120G>C) n.634G>C | |
1 | g.154571205G>T | CA342629904 | CHRNB2 | c.382G>T (p.Glu128Ter) c.388G>T (p.Glu130Ter) c.-9-120G>T (n.-9-120G>T) n.634G>T | |
1 | g.154571206A>C | CA342629905 | CHRNB2 | c.383A>C (p.Glu128Ala) c.389A>C (p.Glu130Ala) c.-9-119A>C (n.-9-119A>C) n.635A>C | |
1 | g.154571206A>G | CA342629906 | CHRNB2 | c.383A>G (p.Glu128Gly) c.389A>G (p.Glu130Gly) c.-9-119A>G (n.-9-119A>G) n.635A>G | |
1 | g.154571206A>T | CA342629907 | CHRNB2 | c.383A>T (p.Glu128Val) c.389A>T (p.Glu130Val) c.-9-119A>T (n.-9-119A>T) n.635A>T | |
1 | g.154571207G>A | CA420970282 | CHRNB2 | c.384G>A (p.Glu128=) c.390G>A (p.Glu130=) c.-9-118G>A (n.-9-118G>A) n.636G>A | dbSNP gnomAD v2 gnomAD v4 |
1 | g.154571207G>C | CA342629908 | CHRNB2 | c.384G>C (p.Glu128Asp) c.390G>C (p.Glu130Asp) c.-9-118G>C (n.-9-118G>C) n.636G>C | |
1 | g.154571207G= | CA2480925184 | CHRNB2 | c.384G= (p.Glu128=) c.390G= (p.Glu130=) c.-9-118G= (n.-9-118G=) n.636G= | |
1 | g.154571207G>T | CA342629909 | CHRNB2 | c.384G>T (p.Glu128Asp) c.390G>T (p.Glu130Asp) c.-9-118G>T (n.-9-118G>T) n.636G>T | COSMIC |
1 | g.154571208G>A | CA342629910 | CHRNB2 | c.385G>A (p.Val129Met) c.391G>A (p.Val131Met) c.-9-117G>A (n.-9-117G>A) n.637G>A | COSMIC |
1 | g.154571208G>C | CA342629911 | CHRNB2 | c.385G>C (p.Val129Leu) c.391G>C (p.Val131Leu) c.-9-117G>C (n.-9-117G>C) n.637G>C | |
1 | g.154571208G>T | CA342629912 | CHRNB2 | c.385G>T (p.Val129Leu) c.391G>T (p.Val131Leu) c.-9-117G>T (n.-9-117G>T) n.637G>T | |
1 | g.154571209T>A | CA342629913 | CHRNB2 | c.386T>A (p.Val129Glu) c.392T>A (p.Val131Glu) c.-9-116T>A (n.-9-116T>A) n.638T>A | |
1 | g.154571209T>C | CA342629914 | CHRNB2 | c.386T>C (p.Val129Ala) c.392T>C (p.Val131Ala) c.-9-116T>C (n.-9-116T>C) n.638T>C | |
1 | g.154571209T>G | CA342629915 | CHRNB2 | c.386T>G (p.Val129Gly) c.392T>G (p.Val131Gly) c.-9-116T>G (n.-9-116T>G) n.638T>G | |
1 | g.154571210G>A | CA420970288 | CHRNB2 | c.387G>A (p.Val129=) c.393G>A (p.Val131=) c.-9-115G>A (n.-9-115G>A) n.639G>A | |
1 | g.154571210G>C | CA420970290 | CHRNB2 | c.387G>C (p.Val129=) c.393G>C (p.Val131=) c.-9-115G>C (n.-9-115G>C) n.639G>C | |
1 | g.154571210G>T | CA420970291 | CHRNB2 | c.387G>T (p.Val129=) c.393G>T (p.Val131=) c.-9-115G>T (n.-9-115G>T) n.639G>T | dbSNP |
1 | g.154571211T>A | CA342629918 | CHRNB2 | c.388T>A (p.Ser130Thr) c.394T>A (p.Ser132Thr) c.-9-114T>A (n.-9-114T>A) n.640T>A | gnomAD v4 |
1 | g.154571211T>C | CA342629917 | CHRNB2 | c.388T>C (p.Ser130Pro) c.394T>C (p.Ser132Pro) c.-9-114T>C (n.-9-114T>C) n.640T>C | |
1 | g.154571211T>G | CA342629916 | CHRNB2 | c.388T>G (p.Ser130Ala) c.394T>G (p.Ser132Ala) c.-9-114T>G (n.-9-114T>G) n.640T>G | gnomAD v4 |
1 | g.154571212C>A | CA342629919 | CHRNB2 | c.389C>A (p.Ser130Tyr) c.395C>A (p.Ser132Tyr) c.-9-113C>A (n.-9-113C>A) n.641C>A | |
1 | g.154571212C>G | CA342629920 | CHRNB2 | c.389C>G (p.Ser130Cys) c.395C>G (p.Ser132Cys) c.-9-113C>G (n.-9-113C>G) n.641C>G | |
1 | g.154571212C>T | CA342629921 | CHRNB2 | c.389C>T (p.Ser130Phe) c.395C>T (p.Ser132Phe) c.-9-113C>T (n.-9-113C>T) n.641C>T | gnomAD v4 |
1 | g.154571212_154571215delinsCCTT | CA2480925185 | CHRNB2 | c.389_392delinsCCTT (p.Ser130=) c.395_398delinsCCTT (p.Ser132=) c.-9-113_-9-110delinsCCTT (n.-9-113_-9-110delinsCCTT) n.641_644delinsCCTT | |
1 | g.154571213C>A | CA420970300 | CHRNB2 | c.390C>A (p.Ser130=) c.396C>A (p.Ser132=) c.-9-112C>A (n.-9-112C>A) n.642C>A | |
1 | g.154571213C>G | CA420970302 | CHRNB2 | c.390C>G (p.Ser130=) c.396C>G (p.Ser132=) c.-9-112C>G (n.-9-112C>G) n.642C>G | |
1 | g.154571213C>T | CA420970303 | CHRNB2 | c.390C>T (p.Ser130=) c.396C>T (p.Ser132=) c.-9-112C>T (n.-9-112C>T) n.642C>T | gnomAD v4 |
1 | g.154571215_154571217del | CA526407534 | CHRNB2 | c.392_394del (p.Phe131del) c.398_400del (p.Phe133del) c.-9-110_-9-108del (n.-9-110_-9-108del) n.644_646del | dbSNP gnomAD v2 gnomAD v4 |
1 | g.154571214T>A | CA342629922 | CHRNB2 | c.391T>A (p.Phe131Ile) c.397T>A (p.Phe133Ile) c.-9-111T>A (n.-9-111T>A) n.643T>A | |
1 | g.154571214T>C | CA342629923 | CHRNB2 | c.391T>C (p.Phe131Leu) c.397T>C (p.Phe133Leu) c.-9-111T>C (n.-9-111T>C) n.643T>C | |
1 | g.154571214T>G | CA342629924 | CHRNB2 | c.391T>G (p.Phe131Val) c.397T>G (p.Phe133Val) c.-9-111T>G (n.-9-111T>G) n.643T>G | |
1 | g.154571215T>A | CA342629925 | CHRNB2 | c.392T>A (p.Phe131Tyr) c.398T>A (p.Phe133Tyr) c.-9-110T>A (n.-9-110T>A) n.644T>A | |
1 | g.154571215T>C | CA342629927 | CHRNB2 | c.392T>C (p.Phe131Ser) c.398T>C (p.Phe133Ser) c.-9-110T>C (n.-9-110T>C) n.644T>C | |
1 | g.154571215T>G | CA342629926 | CHRNB2 | c.392T>G (p.Phe131Cys) c.398T>G (p.Phe133Cys) c.-9-110T>G (n.-9-110T>G) n.644T>G | |
1 | g.154571216C>A | CA342629928 | CHRNB2 | c.393C>A (p.Phe131Leu) c.399C>A (p.Phe133Leu) c.-9-109C>A (n.-9-109C>A) n.645C>A | |
1 | g.154571216C= | CA2480925186 | CHRNB2 | c.393C= (p.Phe131=) c.399C= (p.Phe133=) c.-9-109C= (n.-9-109C=) n.645C= | |
1 | g.154571216C>G | CA342629929 | CHRNB2 | c.393C>G (p.Phe131Leu) c.399C>G (p.Phe133Leu) c.-9-109C>G (n.-9-109C>G) n.645C>G | |
1 | g.154571216C>T | CA1130721 | CHRNB2 | c.393C>T (p.Phe131=) c.399C>T (p.Phe133=) c.-9-109C>T (n.-9-109C>T) n.645C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.154571217T>A | CA342629930 | CHRNB2 | c.394T>A (p.Tyr132Asn) c.400T>A (p.Tyr134Asn) c.-9-108T>A (n.-9-108T>A) n.646T>A | |
1 | g.154571217T>C | CA16616984 | CHRNB2 | c.394T>C (p.Tyr132His) c.400T>C (p.Tyr134His) c.-9-108T>C (n.-9-108T>C) n.646T>C | ClinVar dbSNP gnomAD v4 |
1 | g.154571217T>G | CA342629931 | CHRNB2 | c.394T>G (p.Tyr132Asp) c.400T>G (p.Tyr134Asp) c.-9-108T>G (n.-9-108T>G) n.646T>G | |
1 | g.154571217T= | CA2480925187 | CHRNB2 | c.394T= (p.Tyr132=) c.400T= (p.Tyr134=) c.-9-108T= (n.-9-108T=) n.646T= | |
1 | g.154571218A= | CA1141781775 | CHRNB2 | c.395A= (p.Tyr132=) c.401A= (p.Tyr134=) c.-9-107A= (n.-9-107A=) n.647A= | |
1 | g.154571218A>C | CA342629932 | CHRNB2 | c.395A>C (p.Tyr132Ser) c.401A>C (p.Tyr134Ser) c.-9-107A>C (n.-9-107A>C) n.647A>C | |
1 | g.154571218A>G | CA1130722 | CHRNB2 | c.395A>G (p.Tyr132Cys) c.401A>G (p.Tyr134Cys) c.-9-107A>G (n.-9-107A>G) n.647A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.154571218A>T | CA342629933 | CHRNB2 | c.395A>T (p.Tyr132Phe) c.401A>T (p.Tyr134Phe) c.-9-107A>T (n.-9-107A>T) n.647A>T | |
1 | g.154571219T>A | CA342629934 | CHRNB2 | c.396T>A (p.Tyr132Ter) c.402T>A (p.Tyr134Ter) c.-9-106T>A (n.-9-106T>A) n.648T>A | |
1 | g.154571219T>C | CA420970322 | CHRNB2 | c.396T>C (p.Tyr132=) c.402T>C (p.Tyr134=) c.-9-106T>C (n.-9-106T>C) n.648T>C | |
1 | g.154571219T>G | CA342629935 | CHRNB2 | c.396T>G (p.Tyr132Ter) c.402T>G (p.Tyr134Ter) c.-9-106T>G (n.-9-106T>G) n.648T>G | |
1 | g.154571220T>A | CA342629936 | CHRNB2 | c.397T>A (p.Ser133Thr) c.403T>A (p.Ser135Thr) c.-9-105T>A (n.-9-105T>A) n.649T>A | |
1 | g.154571220T>C | CA30834069 | CHRNB2 | c.397T>C (p.Ser133Pro) c.403T>C (p.Ser135Pro) c.-9-105T>C (n.-9-105T>C) n.649T>C | dbSNP |
1 | g.154571220T>G | CA342629937 | CHRNB2 | c.397T>G (p.Ser133Ala) c.403T>G (p.Ser135Ala) c.-9-105T>G (n.-9-105T>G) n.649T>G | |
1 | g.154571220T= | CA1143378285 | CHRNB2 | c.397T= (p.Ser133=) c.403T= (p.Ser135=) c.-9-105T= (n.-9-105T=) n.649T= | |
1 | g.154571221C>A | CA342629938 | CHRNB2 | c.398C>A (p.Ser133Tyr) c.404C>A (p.Ser135Tyr) c.-9-104C>A (n.-9-104C>A) n.650C>A | |
1 | g.154571221C= | CA2480925188 | CHRNB2 | c.398C= (p.Ser133=) c.404C= (p.Ser135=) c.-9-104C= (n.-9-104C=) n.650C= | |
1 | g.154571221C>G | CA1130723 | CHRNB2 | c.398C>G (p.Ser133Cys) c.404C>G (p.Ser135Cys) c.-9-104C>G (n.-9-104C>G) n.650C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.154571221C>T | CA342629939 | CHRNB2 | c.398C>T (p.Ser133Phe) c.404C>T (p.Ser135Phe) c.-9-104C>T (n.-9-104C>T) n.650C>T | |
1 | g.154571222C>A | CA420970333 | CHRNB2 | c.399C>A (p.Ser133=) c.405C>A (p.Ser135=) c.-9-103C>A (n.-9-103C>A) n.651C>A | gnomAD v4 |
1 | g.154571222C>G | CA420970336 | CHRNB2 | c.399C>G (p.Ser133=) c.405C>G (p.Ser135=) c.-9-103C>G (n.-9-103C>G) n.651C>G | |
1 | g.154571222C>T | CA420970335 | CHRNB2 | c.399C>T (p.Ser133=) c.405C>T (p.Ser135=) c.-9-103C>T (n.-9-103C>T) n.651C>T | gnomAD v4 |
1 | g.154571223A= | CA2480925189 | CHRNB2 | c.400A= (p.Asn134=) c.406A= (p.Asn136=) c.-9-102A= (n.-9-102A=) n.652A= | |
1 | g.154571223A>C | CA342629940 | CHRNB2 | c.400A>C (p.Asn134His) c.406A>C (p.Asn136His) c.-9-102A>C (n.-9-102A>C) n.652A>C | dbSNP gnomAD v3 gnomAD v4 |
1 | g.154571223A>G | CA342629942 | CHRNB2 | c.400A>G (p.Asn134Asp) c.406A>G (p.Asn136Asp) c.-9-102A>G (n.-9-102A>G) n.652A>G | |
1 | g.154571223A>T | CA342629941 | CHRNB2 | c.400A>T (p.Asn134Tyr) c.406A>T (p.Asn136Tyr) c.-9-102A>T (n.-9-102A>T) n.652A>T | |
1 | g.154571224A>C | CA342629943 | CHRNB2 | c.401A>C (p.Asn134Thr) c.407A>C (p.Asn136Thr) c.-9-101A>C (n.-9-101A>C) n.653A>C | |
1 | g.154571224A>G | CA342629944 | CHRNB2 | c.401A>G (p.Asn134Ser) c.407A>G (p.Asn136Ser) c.-9-101A>G (n.-9-101A>G) n.653A>G | ClinVar gnomAD v4 |
1 | g.154571224A>T | CA342629945 | CHRNB2 | c.401A>T (p.Asn134Ile) c.407A>T (p.Asn136Ile) c.-9-101A>T (n.-9-101A>T) n.653A>T | |
1 | g.154571225T>A | CA342629946 | CHRNB2 | c.402T>A (p.Asn134Lys) c.408T>A (p.Asn136Lys) c.-9-100T>A (n.-9-100T>A) n.654T>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.154571225T>C | CA1130724 | CHRNB2 | c.402T>C (p.Asn134=) c.408T>C (p.Asn136=) c.-9-100T>C (n.-9-100T>C) n.654T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.154571225T>G | CA342629947 | CHRNB2 | c.402T>G (p.Asn134Lys) c.408T>G (p.Asn136Lys) c.-9-100T>G (n.-9-100T>G) n.654T>G | |
1 | g.154571225T= | CA2480925190 | CHRNB2 | c.402T= (p.Asn134=) c.408T= (p.Asn136=) c.-9-100T= (n.-9-100T=) n.654T= | |
1 | g.154571226G>A | CA342629948 | CHRNB2 | c.403G>A (p.Ala135Thr) c.409G>A (p.Ala137Thr) c.-9-99G>A (n.-9-99G>A) n.655G>A | gnomAD v4 |
1 | g.154571226G>C | CA342629949 | CHRNB2 | c.403G>C (p.Ala135Pro) c.409G>C (p.Ala137Pro) c.-9-99G>C (n.-9-99G>C) n.655G>C | |
1 | g.154571226G>T | CA342629950 | CHRNB2 | c.403G>T (p.Ala135Ser) c.409G>T (p.Ala137Ser) c.-9-99G>T (n.-9-99G>T) n.655G>T | |
1 | g.154571227C>A | CA342629951 | CHRNB2 | c.404C>A (p.Ala135Asp) c.410C>A (p.Ala137Asp) c.-9-98C>A (n.-9-98C>A) n.656C>A | |
1 | g.154571227C= | CA2480925191 | CHRNB2 | c.404C= (p.Ala135=) c.410C= (p.Ala137=) c.-9-98C= (n.-9-98C=) n.656C= | |
1 | g.154571227C>G | CA342629952 | CHRNB2 | c.404C>G (p.Ala135Gly) c.410C>G (p.Ala137Gly) c.-9-98C>G (n.-9-98C>G) n.656C>G | |
1 | g.154571227C>T | CA16609870 | CHRNB2 | c.404C>T (p.Ala135Val) c.410C>T (p.Ala137Val) c.-9-98C>T (n.-9-98C>T) n.656C>T | ClinVar dbSNP gnomAD v4 COSMIC |
1 | g.154571228C>A | CA420970350 | CHRNB2 | c.405C>A (p.Ala135=) c.411C>A (p.Ala137=) c.-9-97C>A (n.-9-97C>A) n.657C>A | |
1 | g.154571228C= | CA2480925192 | CHRNB2 | c.405C= (p.Ala135=) c.411C= (p.Ala137=) c.-9-97C= (n.-9-97C=) n.657C= | |
1 | g.154571228C>G | CA420970353 | CHRNB2 | c.405C>G (p.Ala135=) c.411C>G (p.Ala137=) c.-9-97C>G (n.-9-97C>G) n.657C>G | ClinVar dbSNP |
1 | g.154571228C>T | CA30834075 | CHRNB2 | c.405C>T (p.Ala135=) c.411C>T (p.Ala137=) c.-9-97C>T (n.-9-97C>T) n.657C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.154571229G>A | CA1130725 | CHRNB2 | c.406G>A (p.Val136Met) c.412G>A (p.Val138Met) c.-9-96G>A (n.-9-96G>A) n.658G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.154571229G>C | CA342629954 | CHRNB2 | c.406G>C (p.Val136Leu) c.412G>C (p.Val138Leu) c.-9-96G>C (n.-9-96G>C) n.658G>C | |
1 | g.154571229G= | CA2480925193 | CHRNB2 | c.406G= (p.Val136=) c.412G= (p.Val138=) c.-9-96G= (n.-9-96G=) n.658G= | |
1 | g.154571229G>T | CA342629953 | CHRNB2 | c.406G>T (p.Val136Leu) c.412G>T (p.Val138Leu) c.-9-96G>T (n.-9-96G>T) n.658G>T | dbSNP |
1 | g.154571230T>A | CA342629955 | CHRNB2 | c.407T>A (p.Val136Glu) c.413T>A (p.Val138Glu) c.-9-95T>A (n.-9-95T>A) n.659T>A | |
1 | g.154571230T>C | CA342629956 | CHRNB2 | c.407T>C (p.Val136Ala) c.413T>C (p.Val138Ala) c.-9-95T>C (n.-9-95T>C) n.659T>C | |
1 | g.154571230T>G | CA342629957 | CHRNB2 | c.407T>G (p.Val136Gly) c.413T>G (p.Val138Gly) c.-9-95T>G (n.-9-95T>G) n.659T>G | |
1 | g.154571231G>A | CA420970359 | CHRNB2 | c.408G>A (p.Val136=) c.414G>A (p.Val138=) c.-9-94G>A (n.-9-94G>A) n.660G>A | |
1 | g.154571231G>C | CA420970360 | CHRNB2 | c.408G>C (p.Val136=) c.414G>C (p.Val138=) c.-9-94G>C (n.-9-94G>C) n.660G>C | |
1 | g.154571231G>T | CA420970362 | CHRNB2 | c.408G>T (p.Val136=) c.414G>T (p.Val138=) c.-9-94G>T (n.-9-94G>T) n.660G>T | |
1 | g.154571232G>A | CA342629958 | CHRNB2 | c.409G>A (p.Val137Ile) c.415G>A (p.Val139Ile) c.-9-93G>A (n.-9-93G>A) n.661G>A | dbSNP gnomAD v2 gnomAD v4 |
1 | g.154571232G>C | CA342629959 | CHRNB2 | c.409G>C (p.Val137Leu) c.415G>C (p.Val139Leu) c.-9-93G>C (n.-9-93G>C) n.661G>C | |
1 | g.154571232G= | CA2480925194 | CHRNB2 | c.409G= (p.Val137=) c.415G= (p.Val139=) c.-9-93G= (n.-9-93G=) n.661G= | |
1 | g.154571232G>T | CA342629960 | CHRNB2 | c.409G>T (p.Val137Phe) c.415G>T (p.Val139Phe) c.-9-93G>T (n.-9-93G>T) n.661G>T | |
1 | g.154571233T>A | CA342629961 | CHRNB2 | c.410T>A (p.Val137Asp) c.416T>A (p.Val139Asp) c.-9-92T>A (n.-9-92T>A) n.662T>A | |
1 | g.154571233T>C | CA1130726 | CHRNB2 | c.410T>C (p.Val137Ala) c.416T>C (p.Val139Ala) c.-9-92T>C (n.-9-92T>C) n.662T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.154571233T>G | CA342629962 | CHRNB2 | c.410T>G (p.Val137Gly) c.416T>G (p.Val139Gly) c.-9-92T>G (n.-9-92T>G) n.662T>G | ClinVar dbSNP gnomAD v4 |
1 | g.154571233T= | CA2480925195 | CHRNB2 | c.410T= (p.Val137=) c.416T= (p.Val139=) c.-9-92T= (n.-9-92T=) n.662T= | |
1 | g.154571234C>A | CA420970369 | CHRNB2 | c.411C>A (p.Val137=) c.417C>A (p.Val139=) c.-9-91C>A (n.-9-91C>A) n.663C>A | |
1 | g.154571234C= | CA1144135311 | CHRNB2 | c.411C= (p.Val137=) c.417C= (p.Val139=) c.-9-91C= (n.-9-91C=) n.663C= | |
1 | g.154571234C>G | CA420970370 | CHRNB2 | c.411C>G (p.Val137=) c.417C>G (p.Val139=) c.-9-91C>G (n.-9-91C>G) n.663C>G | gnomAD v4 |
1 | g.154571234C>T | CA1130727 | CHRNB2 | c.411C>T (p.Val137=) c.417C>T (p.Val139=) c.-9-91C>T (n.-9-91C>T) n.663C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.154571235T>A | CA342629963 | CHRNB2 | c.412T>A (p.Ser138Thr) c.418T>A (p.Ser140Thr) c.-9-90T>A (n.-9-90T>A) n.664T>A | |
1 | g.154571235T>C | CA342629964 | CHRNB2 | c.412T>C (p.Ser138Pro) c.418T>C (p.Ser140Pro) c.-9-90T>C (n.-9-90T>C) n.664T>C | |
1 | g.154571235T>G | CA342629965 | CHRNB2 | c.412T>G (p.Ser138Ala) c.418T>G (p.Ser140Ala) c.-9-90T>G (n.-9-90T>G) n.664T>G | |
1 | g.154571236C>A | CA342629967 | CHRNB2 | c.413C>A (p.Ser138Tyr) c.419C>A (p.Ser140Tyr) c.-9-89C>A (n.-9-89C>A) n.665C>A | |
1 | g.154571236C>G | CA342629968 | CHRNB2 | c.413C>G (p.Ser138Cys) c.419C>G (p.Ser140Cys) c.-9-89C>G (n.-9-89C>G) n.665C>G | |
1 | g.154571236C>T | CA342629966 | CHRNB2 | c.413C>T (p.Ser138Phe) c.419C>T (p.Ser140Phe) c.-9-89C>T (n.-9-89C>T) n.665C>T | |
1 | g.154571237C>A | CA420970377 | CHRNB2 | c.414C>A (p.Ser138=) c.420C>A (p.Ser140=) c.-9-88C>A (n.-9-88C>A) n.666C>A | |
1 | g.154571237C= | CA2480925196 | CHRNB2 | c.414C= (p.Ser138=) c.420C= (p.Ser140=) c.-9-88C= (n.-9-88C=) n.666C= | |
1 | g.154571237C>G | CA420970379 | CHRNB2 | c.414C>G (p.Ser138=) c.420C>G (p.Ser140=) c.-9-88C>G (n.-9-88C>G) n.666C>G | |
1 | g.154571237C>T | CA420970380 | CHRNB2 | c.414C>T (p.Ser138=) c.420C>T (p.Ser140=) c.-9-88C>T (n.-9-88C>T) n.666C>T | dbSNP gnomAD v4 |
1 | g.154571238T>A | CA342629969 | CHRNB2 | c.415T>A (p.Tyr139Asn) c.421T>A (p.Tyr141Asn) c.-9-87T>A (n.-9-87T>A) n.667T>A | |
1 | g.154571238T>C | CA30834090 | CHRNB2 | c.415T>C (p.Tyr139His) c.421T>C (p.Tyr141His) c.-9-87T>C (n.-9-87T>C) n.667T>C | dbSNP |
1 | g.154571238T>G | CA342629970 | CHRNB2 | c.415T>G (p.Tyr139Asp) c.421T>G (p.Tyr141Asp) c.-9-87T>G (n.-9-87T>G) n.667T>G | |
1 | g.154571238T= | CA1143407616 | CHRNB2 | c.415T= (p.Tyr139=) c.421T= (p.Tyr141=) c.-9-87T= (n.-9-87T=) n.667T= | |
1 | g.154571239A= | CA2480925197 | CHRNB2 | c.416A= (p.Tyr139=) c.422A= (p.Tyr141=) c.-9-86A= (n.-9-86A=) n.668A= | |
1 | g.154571239A>C | CA342629971 | CHRNB2 | c.416A>C (p.Tyr139Ser) c.422A>C (p.Tyr141Ser) c.-9-86A>C (n.-9-86A>C) n.668A>C | ClinVar dbSNP |
1 | g.154571239A>G | CA342629972 | CHRNB2 | c.416A>G (p.Tyr139Cys) c.422A>G (p.Tyr141Cys) c.-9-86A>G (n.-9-86A>G) n.668A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.154571239A>T | CA342629973 | CHRNB2 | c.416A>T (p.Tyr139Phe) c.422A>T (p.Tyr141Phe) c.-9-86A>T (n.-9-86A>T) n.668A>T | |
1 | g.154571240T>A | CA342629974 | CHRNB2 | c.417T>A (p.Tyr139Ter) c.423T>A (p.Tyr141Ter) c.-9-85T>A (n.-9-85T>A) n.669T>A | |
1 | g.154571240T>C | CA420970387 | CHRNB2 | c.417T>C (p.Tyr139=) c.423T>C (p.Tyr141=) c.-9-85T>C (n.-9-85T>C) n.669T>C | |
1 | g.154571240T>G | CA342629975 | CHRNB2 | c.417T>G (p.Tyr139Ter) c.423T>G (p.Tyr141Ter) c.-9-85T>G (n.-9-85T>G) n.669T>G | |
1 | g.154571241G>A | CA342629976 | CHRNB2 | c.418G>A (p.Asp140Asn) c.424G>A (p.Asp142Asn) c.-9-84G>A (n.-9-84G>A) n.670G>A | dbSNP gnomAD v2 gnomAD v4 |
1 | g.154571241G>C | CA342629977 | CHRNB2 | c.418G>C (p.Asp140His) c.424G>C (p.Asp142His) c.-9-84G>C (n.-9-84G>C) n.670G>C | |
1 | g.154571241G= | CA2480925198 | CHRNB2 | c.418G= (p.Asp140=) c.424G= (p.Asp142=) c.-9-84G= (n.-9-84G=) n.670G= | |
1 | g.154571241G>T | CA342629978 | CHRNB2 | c.418G>T (p.Asp140Tyr) c.424G>T (p.Asp142Tyr) c.-9-84G>T (n.-9-84G>T) n.670G>T | |
1 | g.154571242A>C | CA342629981 | CHRNB2 | c.419A>C (p.Asp140Ala) c.425A>C (p.Asp142Ala) c.-9-83A>C (n.-9-83A>C) n.671A>C | |
1 | g.154571242A>G | CA342629980 | CHRNB2 | c.419A>G (p.Asp140Gly) c.425A>G (p.Asp142Gly) c.-9-83A>G (n.-9-83A>G) n.671A>G | |
1 | g.154571242A>T | CA342629979 | CHRNB2 | c.419A>T (p.Asp140Val) c.425A>T (p.Asp142Val) c.-9-83A>T (n.-9-83A>T) n.671A>T | |
1 | g.154571243T>A | CA342629982 | CHRNB2 | c.420T>A (p.Asp140Glu) c.426T>A (p.Asp142Glu) c.-9-82T>A (n.-9-82T>A) n.672T>A | |
1 | g.154571243T>C | CA420970395 | CHRNB2 | c.420T>C (p.Asp140=) c.426T>C (p.Asp142=) c.-9-82T>C (n.-9-82T>C) n.672T>C | |
1 | g.154571243T>G | CA342629983 | CHRNB2 | c.420T>G (p.Asp140Glu) c.426T>G (p.Asp142Glu) c.-9-82T>G (n.-9-82T>G) n.672T>G | |
1 | g.154571244G>A | CA342629984 | CHRNB2 | c.421G>A (p.Gly141Ser) c.427G>A (p.Gly143Ser) c.-9-81G>A (n.-9-81G>A) n.673G>A | gnomAD v4 |
1 | g.154571244G>C | CA342629985 | CHRNB2 | c.421G>C (p.Gly141Arg) c.427G>C (p.Gly143Arg) c.-9-81G>C (n.-9-81G>C) n.673G>C | |
1 | g.154571244G>T | CA342629986 | CHRNB2 | c.421G>T (p.Gly141Cys) c.427G>T (p.Gly143Cys) c.-9-81G>T (n.-9-81G>T) n.673G>T | |
1 | g.154571245G>A | CA30834098 | CHRNB2 | c.422G>A (p.Gly141Asp) c.428G>A (p.Gly143Asp) c.-9-80G>A (n.-9-80G>A) n.674G>A | dbSNP |
1 | g.154571245G>C | CA342629987 | CHRNB2 | c.422G>C (p.Gly141Ala) c.428G>C (p.Gly143Ala) c.-9-80G>C (n.-9-80G>C) n.674G>C | |
1 | g.154571245G= | CA1143489856 | CHRNB2 | c.422G= (p.Gly141=) c.428G= (p.Gly143=) c.-9-80G= (n.-9-80G=) n.674G= | |
1 | g.154571245G>T | CA342629988 | CHRNB2 | c.422G>T (p.Gly141Val) c.428G>T (p.Gly143Val) c.-9-80G>T (n.-9-80G>T) n.674G>T | COSMIC |
1 | g.154571246C>A | CA420970401 | CHRNB2 | c.423C>A (p.Gly141=) c.429C>A (p.Gly143=) c.-9-79C>A (n.-9-79C>A) n.675C>A | gnomAD v4 |
1 | g.154571246C= | CA2480925199 | CHRNB2 | c.423C= (p.Gly141=) c.429C= (p.Gly143=) c.-9-79C= (n.-9-79C=) n.675C= | |
1 | g.154571246C>G | CA420970403 | CHRNB2 | c.423C>G (p.Gly141=) c.429C>G (p.Gly143=) c.-9-79C>G (n.-9-79C>G) n.675C>G | |
1 | g.154571246C>T | CA420970404 | CHRNB2 | c.423C>T (p.Gly141=) c.429C>T (p.Gly143=) c.-9-79C>T (n.-9-79C>T) n.675C>T | ClinVar dbSNP gnomAD v4 |
1 | g.154571247A>C | CA342629989 | CHRNB2 | c.424A>C (p.Ser142Arg) c.430A>C (p.Ser144Arg) c.-9-78A>C (n.-9-78A>C) n.676A>C | |
1 | g.154571247A>G | CA342629990 | CHRNB2 | c.424A>G (p.Ser142Gly) c.430A>G (p.Ser144Gly) c.-9-78A>G (n.-9-78A>G) n.676A>G | |
1 | g.154571247A>T | CA342629991 | CHRNB2 | c.424A>T (p.Ser142Cys) c.430A>T (p.Ser144Cys) c.-9-78A>T (n.-9-78A>T) n.676A>T | |
1 | g.154571248G>A | CA342629994 | CHRNB2 | c.425G>A (p.Ser142Asn) c.431G>A (p.Ser144Asn) c.-9-77G>A (n.-9-77G>A) n.677G>A | |
1 | g.154571248G>C | CA342629993 | CHRNB2 | c.425G>C (p.Ser142Thr) c.431G>C (p.Ser144Thr) c.-9-77G>C (n.-9-77G>C) n.677G>C | |
1 | g.154571248G>T | CA342629992 | CHRNB2 | c.425G>T (p.Ser142Ile) c.431G>T (p.Ser144Ile) c.-9-77G>T (n.-9-77G>T) n.677G>T | |
1 | g.154571249C>A | CA342629995 | CHRNB2 | c.426C>A (p.Ser142Arg) c.432C>A (p.Ser144Arg) c.-9-76C>A (n.-9-76C>A) n.678C>A | |
1 | g.154571249C>G | CA342629996 | CHRNB2 | c.426C>G (p.Ser142Arg) c.432C>G (p.Ser144Arg) c.-9-76C>G (n.-9-76C>G) n.678C>G | |
1 | g.154571249C>T | CA420970411 | CHRNB2 | c.426C>T (p.Ser142=) c.432C>T (p.Ser144=) c.-9-76C>T (n.-9-76C>T) n.678C>T | COSMIC |
1 | g.154571250A>C | CA342629997 | CHRNB2 | c.427A>C (p.Ile143Leu) c.433A>C (p.Ile145Leu) c.-9-75A>C (n.-9-75A>C) n.679A>C | |
1 | g.154571250A>G | CA342629998 | CHRNB2 | c.427A>G (p.Ile143Val) c.433A>G (p.Ile145Val) c.-9-75A>G (n.-9-75A>G) n.679A>G | dbSNP |
1 | g.154571250A>T | CA342629999 | CHRNB2 | c.427A>T (p.Ile143Phe) c.433A>T (p.Ile145Phe) c.-9-75A>T (n.-9-75A>T) n.679A>T | |
1 | g.154571251T>A | CA342630000 | CHRNB2 | c.428T>A (p.Ile143Asn) c.434T>A (p.Ile145Asn) c.-9-74T>A (n.-9-74T>A) n.680T>A | |
1 | g.154571251T>C | CA342630001 | CHRNB2 | c.428T>C (p.Ile143Thr) c.434T>C (p.Ile145Thr) c.-9-74T>C (n.-9-74T>C) n.680T>C | |
1 | g.154571251T>G | CA342630002 | CHRNB2 | c.428T>G (p.Ile143Ser) c.434T>G (p.Ile145Ser) c.-9-74T>G (n.-9-74T>G) n.680T>G | |
1 | g.154571252C>A | CA420970418 | CHRNB2 | c.429C>A (p.Ile143=) c.435C>A (p.Ile145=) c.-9-73C>A (n.-9-73C>A) n.681C>A | |
1 | g.154571252C= | CA1143652181 | CHRNB2 | c.429C= (p.Ile143=) c.435C= (p.Ile145=) c.-9-73C= (n.-9-73C=) n.681C= | |
1 | g.154571252C>G | CA342630003 | CHRNB2 | c.429C>G (p.Ile143Met) c.435C>G (p.Ile145Met) c.-9-73C>G (n.-9-73C>G) n.681C>G | |
1 | g.154571252C>T | CA1130728 | CHRNB2 | c.429C>T (p.Ile143=) c.435C>T (p.Ile145=) c.-9-73C>T (n.-9-73C>T) n.681C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.154571253T>A | CA342630004 | CHRNB2 | c.430T>A (p.Phe144Ile) c.436T>A (p.Phe146Ile) c.-9-72T>A (n.-9-72T>A) n.682T>A | |
1 | g.154571253T>C | CA342630005 | CHRNB2 | c.430T>C (p.Phe144Leu) c.436T>C (p.Phe146Leu) c.-9-72T>C (n.-9-72T>C) n.682T>C | gnomAD v4 |
1 | g.154571253T>G | CA342630006 | CHRNB2 | c.430T>G (p.Phe144Val) c.436T>G (p.Phe146Val) c.-9-72T>G (n.-9-72T>G) n.682T>G | |
1 | g.154571254T>A | CA342630009 | CHRNB2 | c.431T>A (p.Phe144Tyr) c.437T>A (p.Phe146Tyr) c.-9-71T>A (n.-9-71T>A) n.683T>A | |
1 | g.154571254T>C | CA342630008 | CHRNB2 | c.431T>C (p.Phe144Ser) c.437T>C (p.Phe146Ser) c.-9-71T>C (n.-9-71T>C) n.683T>C | |
1 | g.154571254T>G | CA342630007 | CHRNB2 | c.431T>G (p.Phe144Cys) c.437T>G (p.Phe146Cys) c.-9-71T>G (n.-9-71T>G) n.683T>G | |
1 | g.154571255C>A | CA342630010 | CHRNB2 | c.432C>A (p.Phe144Leu) c.438C>A (p.Phe146Leu) c.-9-70C>A (n.-9-70C>A) n.684C>A | |
1 | g.154571255C= | CA1143358396 | CHRNB2 | c.432C= (p.Phe144=) c.438C= (p.Phe146=) c.-9-70C= (n.-9-70C=) n.684C= | |
1 | g.154571255C>G | CA342630011 | CHRNB2 | c.432C>G (p.Phe144Leu) c.438C>G (p.Phe146Leu) c.-9-70C>G (n.-9-70C>G) n.684C>G | |
1 | g.154571255C>T | CA1130729 | CHRNB2 | c.432C>T (p.Phe144=) c.438C>T (p.Phe146=) c.-9-70C>T (n.-9-70C>T) n.684C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.154571256T>A | CA342630012 | CHRNB2 | c.433T>A (p.Trp145Arg) c.439T>A (p.Trp147Arg) c.-9-69T>A (n.-9-69T>A) n.685T>A | |
1 | g.154571256T>C | CA342630013 | CHRNB2 | c.433T>C (p.Trp145Arg) c.439T>C (p.Trp147Arg) c.-9-69T>C (n.-9-69T>C) n.685T>C | |
1 | g.154571256T>G | CA342630014 | CHRNB2 | c.433T>G (p.Trp145Gly) c.439T>G (p.Trp147Gly) c.-9-69T>G (n.-9-69T>G) n.685T>G | |
1 | g.154571257G>A | CA342630015 | CHRNB2 | c.434G>A (p.Trp145Ter) c.440G>A (p.Trp147Ter) c.-9-68G>A (n.-9-68G>A) n.686G>A | |
1 | g.154571257G>C | CA342630016 | CHRNB2 | c.434G>C (p.Trp145Ser) c.440G>C (p.Trp147Ser) c.-9-68G>C (n.-9-68G>C) n.686G>C | |
1 | g.154571257G>T | CA342630017 | CHRNB2 | c.434G>T (p.Trp145Leu) c.440G>T (p.Trp147Leu) c.-9-68G>T (n.-9-68G>T) n.686G>T | |
1 | g.154571258G>A | CA342630018 | CHRNB2 | c.435G>A (p.Trp145Ter) c.441G>A (p.Trp147Ter) c.-9-67G>A (n.-9-67G>A) n.687G>A | |
1 | g.154571258G>C | CA342630019 | CHRNB2 | c.435G>C (p.Trp145Cys) c.441G>C (p.Trp147Cys) c.-9-67G>C (n.-9-67G>C) n.687G>C | |
1 | g.154571258G>T | CA342630020 | CHRNB2 | c.435G>T (p.Trp145Cys) c.441G>T (p.Trp147Cys) c.-9-67G>T (n.-9-67G>T) n.687G>T | |
1 | g.154571259C>A | CA342630021 | CHRNB2 | c.436C>A (p.Leu146Met) c.442C>A (p.Leu148Met) c.-9-66C>A (n.-9-66C>A) n.688C>A | |
1 | g.154571259C>G | CA342630022 | CHRNB2 | c.436C>G (p.Leu146Val) c.442C>G (p.Leu148Val) c.-9-66C>G (n.-9-66C>G) n.688C>G | |
1 | g.154571259C>T | CA420970435 | CHRNB2 | c.436C>T (p.Leu146=) c.442C>T (p.Leu148=) c.-9-66C>T (n.-9-66C>T) n.688C>T | |
1 | g.154571260T>A | CA342630024 | CHRNB2 | c.437T>A (p.Leu146Gln) c.443T>A (p.Leu148Gln) c.-9-65T>A (n.-9-65T>A) n.689T>A | |
1 | g.154571260T>C | CA342630025 | CHRNB2 | c.437T>C (p.Leu146Pro) c.443T>C (p.Leu148Pro) c.-9-65T>C (n.-9-65T>C) n.689T>C | |
1 | g.154571260T>G | CA342630023 | CHRNB2 | c.437T>G (p.Leu146Arg) c.443T>G (p.Leu148Arg) c.-9-65T>G (n.-9-65T>G) n.689T>G | |
1 | g.154571261G>A | CA1130730 | CHRNB2 | c.438G>A (p.Leu146=) c.444G>A (p.Leu148=) c.-9-64G>A (n.-9-64G>A) n.690G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.154571261G>C | CA420970440 | CHRNB2 | c.438G>C (p.Leu146=) c.444G>C (p.Leu148=) c.-9-64G>C (n.-9-64G>C) n.690G>C | |
1 | g.154571261G= | CA2480925200 | CHRNB2 | c.438G= (p.Leu146=) c.444G= (p.Leu148=) c.-9-64G= (n.-9-64G=) n.690G= | |
1 | g.154571261G>T | CA420970442 | CHRNB2 | c.438G>T (p.Leu146=) c.444G>T (p.Leu148=) c.-9-64G>T (n.-9-64G>T) n.690G>T | |
1 | g.154571262C>A | CA342630026 | CHRNB2 | c.439C>A (p.Pro147Thr) c.445C>A (p.Pro149Thr) c.-9-63C>A (n.-9-63C>A) n.691C>A | |
1 | g.154571262C>G | CA342630027 | CHRNB2 | c.439C>G (p.Pro147Ala) c.445C>G (p.Pro149Ala) c.-9-63C>G (n.-9-63C>G) n.691C>G | |
1 | g.154571262C>T | CA342630028 | CHRNB2 | c.439C>T (p.Pro147Ser) c.445C>T (p.Pro149Ser) c.-9-63C>T (n.-9-63C>T) n.691C>T | |
1 | g.154571263C>A | CA342630029 | CHRNB2 | c.440C>A (p.Pro147Gln) c.446C>A (p.Pro149Gln) c.-9-62C>A (n.-9-62C>A) n.692C>A | |
1 | g.154571263C= | CA1147135256 | CHRNB2 | c.440C= (p.Pro147=) c.446C= (p.Pro149=) c.-9-62C= (n.-9-62C=) n.692C= | |
1 | g.154571263C>G | CA342630030 | CHRNB2 | c.440C>G (p.Pro147Arg) c.446C>G (p.Pro149Arg) c.-9-62C>G (n.-9-62C>G) n.692C>G | |
1 | g.154571263C>T | CA30834116 | CHRNB2 | c.440C>T (p.Pro147Leu) c.446C>T (p.Pro149Leu) c.-9-62C>T (n.-9-62C>T) n.692C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.154571264G>A | CA420970450 | CHRNB2 | c.441G>A (p.Pro147=) c.447G>A (p.Pro149=) c.-9-61G>A (n.-9-61G>A) n.693G>A | ClinVar dbSNP gnomAD v4 COSMIC |
1 | g.154571264G>C | CA420970449 | CHRNB2 | c.441G>C (p.Pro147=) c.447G>C (p.Pro149=) c.-9-61G>C (n.-9-61G>C) n.693G>C | |
1 | g.154571264G= | CA2480925201 | CHRNB2 | c.441G= (p.Pro147=) c.447G= (p.Pro149=) c.-9-61G= (n.-9-61G=) n.693G= | |
1 | g.154571264G>T | CA1130731 | CHRNB2 | c.441G>T (p.Pro147=) c.447G>T (p.Pro149=) c.-9-61G>T (n.-9-61G>T) n.693G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.154571265C>A | CA342630031 | CHRNB2 | c.442C>A (p.Pro148Thr) c.448C>A (p.Pro150Thr) c.-9-60C>A (n.-9-60C>A) n.694C>A | |
1 | g.154571265C>G | CA342630032 | CHRNB2 | c.442C>G (p.Pro148Ala) c.448C>G (p.Pro150Ala) c.-9-60C>G (n.-9-60C>G) n.694C>G | |
1 | g.154571265C>T | CA342630033 | CHRNB2 | c.442C>T (p.Pro148Ser) c.448C>T (p.Pro150Ser) c.-9-60C>T (n.-9-60C>T) n.694C>T | gnomAD v4 |
1 | g.154571266C>A | CA342630035 | CHRNB2 | c.443C>A (p.Pro148His) c.449C>A (p.Pro150His) c.-9-59C>A (n.-9-59C>A) n.695C>A | |
1 | g.154571266C= | CA1148456174 | CHRNB2 | c.443C= (p.Pro148=) c.449C= (p.Pro150=) c.-9-59C= (n.-9-59C=) n.695C= | |
1 | g.154571266C>G | CA1130732 | CHRNB2 | c.443C>G (p.Pro148Arg) c.449C>G (p.Pro150Arg) c.-9-59C>G (n.-9-59C>G) n.695C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.154571266C>T | CA342630034 | CHRNB2 | c.443C>T (p.Pro148Leu) c.449C>T (p.Pro150Leu) c.-9-59C>T (n.-9-59C>T) n.695C>T | |
1 | g.154571267T>A | CA421230798 | CHRNB2 | c.444T>A (p.Pro148=) c.450T>A (p.Pro150=) c.-9-58T>A (n.-9-58T>A) n.696T>A | |
1 | g.154571267T>C | CA421230799 | CHRNB2 | c.444T>C (p.Pro148=) c.450T>C (p.Pro150=) c.-9-58T>C (n.-9-58T>C) n.696T>C | |
1 | g.154571267T>G | CA421230800 | CHRNB2 | c.444T>G (p.Pro148=) c.450T>G (p.Pro150=) c.-9-58T>G (n.-9-58T>G) n.696T>G | |
1 | g.154571268G>A | CA342630036 | CHRNB2 | c.445G>A (p.Ala149Thr) c.451G>A (p.Ala151Thr) c.-9-57G>A (n.-9-57G>A) n.697G>A | COSMIC |
1 | g.154571268G>C | CA342630037 | CHRNB2 | c.445G>C (p.Ala149Pro) c.451G>C (p.Ala151Pro) c.-9-57G>C (n.-9-57G>C) n.697G>C | |
1 | g.154571268G>T | CA342630038 | CHRNB2 | c.445G>T (p.Ala149Ser) c.451G>T (p.Ala151Ser) c.-9-57G>T (n.-9-57G>T) n.697G>T | |
1 | g.154571269C>A | CA342630039 | CHRNB2 | c.446C>A (p.Ala149Asp) c.452C>A (p.Ala151Asp) c.-9-56C>A (n.-9-56C>A) n.698C>A | |
1 | g.154571269C>G | CA342630040 | CHRNB2 | c.446C>G (p.Ala149Gly) c.452C>G (p.Ala151Gly) c.-9-56C>G (n.-9-56C>G) n.698C>G | |
1 | g.154571269C>T | CA342630041 | CHRNB2 | c.446C>T (p.Ala149Val) c.452C>T (p.Ala151Val) c.-9-56C>T (n.-9-56C>T) n.698C>T | |
1 | g.154571270C>A | CA421230802 | CHRNB2 | c.447C>A (p.Ala149=) c.453C>A (p.Ala151=) c.-9-55C>A (n.-9-55C>A) n.699C>A | |
1 | g.154571270C= | CA2480925202 | CHRNB2 | c.447C= (p.Ala149=) c.453C= (p.Ala151=) c.-9-55C= (n.-9-55C=) n.699C= | |
1 | g.154571270C>G | CA421230803 | CHRNB2 | c.447C>G (p.Ala149=) c.453C>G (p.Ala151=) c.-9-55C>G (n.-9-55C>G) n.699C>G | |
1 | g.154571270C>T | CA1130733 | CHRNB2 | c.447C>T (p.Ala149=) c.453C>T (p.Ala151=) c.-9-55C>T (n.-9-55C>T) n.699C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.154571271A= | CA2480925203 | CHRNB2 | c.448A= (p.Ile150=) c.454A= (p.Ile152=) c.-9-54A= (n.-9-54A=) n.700A= | |
1 | g.154571271A>C | CA342630042 | CHRNB2 | c.448A>C (p.Ile150Leu) c.454A>C (p.Ile152Leu) c.-9-54A>C (n.-9-54A>C) n.700A>C | |
1 | g.154571271A>G | CA342630043 | CHRNB2 | c.448A>G (p.Ile150Val) c.454A>G (p.Ile152Val) c.-9-54A>G (n.-9-54A>G) n.700A>G | ClinVar dbSNP |
1 | g.154571271A>T | CA342630044 | CHRNB2 | c.448A>T (p.Ile150Phe) c.454A>T (p.Ile152Phe) c.-9-54A>T (n.-9-54A>T) n.700A>T | |
1 | g.154571272T>A | CA342630045 | CHRNB2 | c.449T>A (p.Ile150Asn) c.455T>A (p.Ile152Asn) c.-9-53T>A (n.-9-53T>A) n.701T>A | dbSNP gnomAD v2 gnomAD v4 |
1 | g.154571272T>C | CA342630046 | CHRNB2 | c.449T>C (p.Ile150Thr) c.455T>C (p.Ile152Thr) c.-9-53T>C (n.-9-53T>C) n.701T>C | |
1 | g.154571272T>G | CA342630047 | CHRNB2 | c.449T>G (p.Ile150Ser) c.455T>G (p.Ile152Ser) c.-9-53T>G (n.-9-53T>G) n.701T>G | |
1 | g.154571272T= | CA2480925204 | CHRNB2 | c.449T= (p.Ile150=) c.455T= (p.Ile152=) c.-9-53T= (n.-9-53T=) n.701T= | |
1 | g.154571273C>A | CA421230812 | CHRNB2 | c.450C>A (p.Ile150=) c.456C>A (p.Ile152=) c.-9-52C>A (n.-9-52C>A) n.702C>A | |
1 | g.154571273C>G | CA342630048 | CHRNB2 | c.450C>G (p.Ile150Met) c.456C>G (p.Ile152Met) c.-9-52C>G (n.-9-52C>G) n.702C>G | |
1 | g.154571273C>T | CA421230813 | CHRNB2 | c.450C>T (p.Ile150=) c.456C>T (p.Ile152=) c.-9-52C>T (n.-9-52C>T) n.702C>T | |
1 | g.154571274T>A | CA342630051 | CHRNB2 | c.451T>A (p.Tyr151Asn) c.457T>A (p.Tyr153Asn) c.-9-51T>A (n.-9-51T>A) n.703T>A | |
1 | g.154571274T>C | CA342630049 | CHRNB2 | c.451T>C (p.Tyr151His) c.457T>C (p.Tyr153His) c.-9-51T>C (n.-9-51T>C) n.703T>C | |
1 | g.154571274T>G | CA342630050 | CHRNB2 | c.451T>G (p.Tyr151Asp) c.457T>G (p.Tyr153Asp) c.-9-51T>G (n.-9-51T>G) n.703T>G | |
1 | g.154571275A= | CA2480925205 | CHRNB2 | c.452A= (p.Tyr151=) c.458A= (p.Tyr153=) c.-9-50A= (n.-9-50A=) n.704A= | |
1 | g.154571275A>C | CA342630052 | CHRNB2 | c.452A>C (p.Tyr151Ser) c.458A>C (p.Tyr153Ser) c.-9-50A>C (n.-9-50A>C) n.704A>C | |
1 | g.154571275A>G | CA342630053 | CHRNB2 | c.452A>G (p.Tyr151Cys) c.458A>G (p.Tyr153Cys) c.-9-50A>G (n.-9-50A>G) n.704A>G | dbSNP |
1 | g.154571275A>T | CA342630054 | CHRNB2 | c.452A>T (p.Tyr151Phe) c.458A>T (p.Tyr153Phe) c.-9-50A>T (n.-9-50A>T) n.704A>T | |
1 | g.154571276C>A | CA342630055 | CHRNB2 | c.453C>A (p.Tyr151Ter) c.459C>A (p.Tyr153Ter) c.-9-49C>A (n.-9-49C>A) n.705C>A | |
1 | g.154571276C= | CA2480925206 | CHRNB2 | c.453C= (p.Tyr151=) c.459C= (p.Tyr153=) c.-9-49C= (n.-9-49C=) n.705C= | |
1 | g.154571276C>G | CA342630056 | CHRNB2 | c.453C>G (p.Tyr151Ter) c.459C>G (p.Tyr153Ter) c.-9-49C>G (n.-9-49C>G) n.705C>G | |
1 | g.154571276C>T | CA1130734 | CHRNB2 | c.453C>T (p.Tyr151=) c.459C>T (p.Tyr153=) c.-9-49C>T (n.-9-49C>T) n.705C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.154571277A>C | CA342630057 | CHRNB2 | c.454A>C (p.Lys152Gln) c.460A>C (p.Lys154Gln) c.-9-48A>C (n.-9-48A>C) n.706A>C | |
1 | g.154571277A>G | CA342630059 | CHRNB2 | c.454A>G (p.Lys152Glu) c.460A>G (p.Lys154Glu) c.-9-48A>G (n.-9-48A>G) n.706A>G | |
1 | g.154571277A>T | CA342630058 | CHRNB2 | c.454A>T (p.Lys152Ter) c.460A>T (p.Lys154Ter) c.-9-48A>T (n.-9-48A>T) n.706A>T | |
1 | g.154571278A= | CA2480925207 | CHRNB2 | c.455A= (p.Lys152=) c.461A= (p.Lys154=) c.-9-47A= (n.-9-47A=) n.707A= | |
1 | g.154571278A>C | CA342630060 | CHRNB2 | c.455A>C (p.Lys152Thr) c.461A>C (p.Lys154Thr) c.-9-47A>C (n.-9-47A>C) n.707A>C | |
1 | g.154571278A>G | CA342630061 | CHRNB2 | c.455A>G (p.Lys152Arg) c.461A>G (p.Lys154Arg) c.-9-47A>G (n.-9-47A>G) n.707A>G | dbSNP gnomAD v4 |
1 | g.154571278A>T | CA342630062 | CHRNB2 | c.455A>T (p.Lys152Met) c.461A>T (p.Lys154Met) c.-9-47A>T (n.-9-47A>T) n.707A>T | |
1 | g.154571279G>A | CA421230815 | CHRNB2 | c.456G>A (p.Lys152=) c.462G>A (p.Lys154=) c.-9-46G>A (n.-9-46G>A) n.708G>A | ClinVar dbSNP gnomAD v4 |
1 | g.154571279G>C | CA342630063 | CHRNB2 | c.456G>C (p.Lys152Asn) c.462G>C (p.Lys154Asn) c.-9-46G>C (n.-9-46G>C) n.708G>C | |
1 | g.154571279G>T | CA342630064 | CHRNB2 | c.456G>T (p.Lys152Asn) c.462G>T (p.Lys154Asn) c.-9-46G>T (n.-9-46G>T) n.708G>T | |
1 | g.154571280A>C | CA342630065 | CHRNB2 | c.457A>C (p.Ser153Arg) c.463A>C (p.Ser155Arg) c.-9-45A>C (n.-9-45A>C) n.709A>C | |
1 | g.154571280A>G | CA342630067 | CHRNB2 | c.457A>G (p.Ser153Gly) c.463A>G (p.Ser155Gly) c.-9-45A>G (n.-9-45A>G) n.709A>G | |
1 | g.154571280A>T | CA342630066 | CHRNB2 | c.457A>T (p.Ser153Cys) c.463A>T (p.Ser155Cys) c.-9-45A>T (n.-9-45A>T) n.709A>T | |
1 | g.154571281G>A | CA342630068 | CHRNB2 | c.458G>A (p.Ser153Asn) c.464G>A (p.Ser155Asn) c.-9-44G>A (n.-9-44G>A) n.710G>A | |
1 | g.154571281G>C | CA342630069 | CHRNB2 | c.458G>C (p.Ser153Thr) c.464G>C (p.Ser155Thr) c.-9-44G>C (n.-9-44G>C) n.710G>C | |
1 | g.154571281G>T | CA342630070 | CHRNB2 | c.458G>T (p.Ser153Ile) c.464G>T (p.Ser155Ile) c.-9-44G>T (n.-9-44G>T) n.710G>T | |
1 | g.154571282C>A | CA342630071 | CHRNB2 | c.459C>A (p.Ser153Arg) c.465C>A (p.Ser155Arg) c.-9-43C>A (n.-9-43C>A) n.711C>A | |
1 | g.154571282C= | CA1145092484 | CHRNB2 | c.459C= (p.Ser153=) c.465C= (p.Ser155=) c.-9-43C= (n.-9-43C=) n.711C= | |
1 | g.154571282C>G | CA1130735 | CHRNB2 | c.459C>G (p.Ser153Arg) c.465C>G (p.Ser155Arg) c.-9-43C>G (n.-9-43C>G) n.711C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.154571282C>T | CA30834133 | CHRNB2 | c.459C>T (p.Ser153=) c.465C>T (p.Ser155=) c.-9-43C>T (n.-9-43C>T) n.711C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.154571283G>A | CA1130736 | CHRNB2 | c.460G>A (p.Ala154Thr) c.466G>A (p.Ala156Thr) c.-9-42G>A (n.-9-42G>A) n.712G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.154571283G>C | CA342630072 | CHRNB2 | c.460G>C (p.Ala154Pro) c.466G>C (p.Ala156Pro) c.-9-42G>C (n.-9-42G>C) n.712G>C | |
1 | g.154571283G= | CA2480925208 | CHRNB2 | c.460G= (p.Ala154=) c.466G= (p.Ala156=) c.-9-42G= (n.-9-42G=) n.712G= | |
1 | g.154571283G>T | CA342630073 | CHRNB2 | c.460G>T (p.Ala154Ser) c.466G>T (p.Ala156Ser) c.-9-42G>T (n.-9-42G>T) n.712G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.154571284C>A | CA342630074 | CHRNB2 | c.461C>A (p.Ala154Glu) c.467C>A (p.Ala156Glu) c.-9-41C>A (n.-9-41C>A) n.713C>A | |
1 | g.154571284C>G | CA342630075 | CHRNB2 | c.461C>G (p.Ala154Gly) c.467C>G (p.Ala156Gly) c.-9-41C>G (n.-9-41C>G) n.713C>G | |
1 | g.154571284C>T | CA342630076 | CHRNB2 | c.461C>T (p.Ala154Val) c.467C>T (p.Ala156Val) c.-9-41C>T (n.-9-41C>T) n.713C>T | |
1 | g.154571285A= | CA2480925209 | CHRNB2 | c.462A= (p.Ala154=) c.468A= (p.Ala156=) c.-9-40A= (n.-9-40A=) n.714A= | |
1 | g.154571285A>C | CA421230829 | CHRNB2 | c.462A>C (p.Ala154=) c.468A>C (p.Ala156=) c.-9-40A>C (n.-9-40A>C) n.714A>C | |
1 | g.154571285A>G | CA421230830 | CHRNB2 | c.462A>G (p.Ala154=) c.468A>G (p.Ala156=) c.-9-40A>G (n.-9-40A>G) n.714A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.154571285A>T | CA421230832 | CHRNB2 | c.462A>T (p.Ala154=) c.468A>T (p.Ala156=) c.-9-40A>T (n.-9-40A>T) n.714A>T | |
1 | g.154571286T>A | CA342630077 | CHRNB2 | c.463T>A (p.Cys155Ser) c.469T>A (p.Cys157Ser) c.-9-39T>A (n.-9-39T>A) n.715T>A | gnomAD v4 |
1 | g.154571286T>C | CA342630079 | CHRNB2 | c.463T>C (p.Cys155Arg) c.469T>C (p.Cys157Arg) c.-9-39T>C (n.-9-39T>C) n.715T>C | COSMIC |
1 | g.154571286T>G | CA342630078 | CHRNB2 | c.463T>G (p.Cys155Gly) c.469T>G (p.Cys157Gly) c.-9-39T>G (n.-9-39T>G) n.715T>G | |
1 | g.154571287G>A | CA342630080 | CHRNB2 | c.464G>A (p.Cys155Tyr) c.470G>A (p.Cys157Tyr) c.-9-38G>A (n.-9-38G>A) n.716G>A | gnomAD v4 |
1 | g.154571287G>C | CA342630081 | CHRNB2 | c.464G>C (p.Cys155Ser) c.470G>C (p.Cys157Ser) c.-9-38G>C (n.-9-38G>C) n.716G>C | |
1 | g.154571287G>T | CA342630082 | CHRNB2 | c.464G>T (p.Cys155Phe) c.470G>T (p.Cys157Phe) c.-9-38G>T (n.-9-38G>T) n.716G>T | |
1 | g.154571288C>A | CA342630083 | CHRNB2 | c.465C>A (p.Cys155Ter) c.471C>A (p.Cys157Ter) c.-9-37C>A (n.-9-37C>A) n.717C>A | |
1 | g.154571288C>G | CA342630084 | CHRNB2 | c.465C>G (p.Cys155Trp) c.471C>G (p.Cys157Trp) c.-9-37C>G (n.-9-37C>G) n.717C>G | |
1 | g.154571288C>T | CA421230835 | CHRNB2 | c.465C>T (p.Cys155=) c.471C>T (p.Cys157=) c.-9-37C>T (n.-9-37C>T) n.717C>T | |
1 | g.154571289A>C | CA342630085 | CHRNB2 | c.466A>C (p.Lys156Gln) c.472A>C (p.Lys158Gln) c.-9-36A>C (n.-9-36A>C) n.718A>C | |
1 | g.154571289A>G | CA342630086 | CHRNB2 | c.466A>G (p.Lys156Glu) c.472A>G (p.Lys158Glu) c.-9-36A>G (n.-9-36A>G) n.718A>G | ClinVar |
1 | g.154571289A>T | CA342630087 | CHRNB2 | c.466A>T (p.Lys156Ter) c.472A>T (p.Lys158Ter) c.-9-36A>T (n.-9-36A>T) n.718A>T | |
1 | g.154571290A>C | CA342630088 | CHRNB2 | c.467A>C (p.Lys156Thr) c.473A>C (p.Lys158Thr) c.-9-35A>C (n.-9-35A>C) n.719A>C | |
1 | g.154571290A>G | CA342630089 | CHRNB2 | c.467A>G (p.Lys156Arg) c.473A>G (p.Lys158Arg) c.-9-35A>G (n.-9-35A>G) n.719A>G | |
1 | g.154571290A>T | CA342630090 | CHRNB2 | c.467A>T (p.Lys156Met) c.473A>T (p.Lys158Met) c.-9-35A>T (n.-9-35A>T) n.719A>T | |
1 | g.154571291G>A | CA421230837 | CHRNB2 | c.468G>A (p.Lys156=) c.474G>A (p.Lys158=) c.-9-34G>A (n.-9-34G>A) n.720G>A | |
1 | g.154571291G>C | CA342630091 | CHRNB2 | c.468G>C (p.Lys156Asn) c.474G>C (p.Lys158Asn) c.-9-34G>C (n.-9-34G>C) n.720G>C | gnomAD v4 COSMIC |
1 | g.154571291G>T | CA342630092 | CHRNB2 | c.468G>T (p.Lys156Asn) c.474G>T (p.Lys158Asn) c.-9-34G>T (n.-9-34G>T) n.720G>T | |
1 | g.154571292A>C | CA342630095 | CHRNB2 | c.469A>C (p.Ile157Leu) c.475A>C (p.Ile159Leu) c.-9-33A>C (n.-9-33A>C) n.721A>C | |
1 | g.154571292A>G | CA342630093 | CHRNB2 | c.469A>G (p.Ile157Val) c.475A>G (p.Ile159Val) c.-9-33A>G (n.-9-33A>G) n.721A>G | |
1 | g.154571292A>T | CA342630094 | CHRNB2 | c.469A>T (p.Ile157Phe) c.475A>T (p.Ile159Phe) c.-9-33A>T (n.-9-33A>T) n.721A>T | gnomAD v4 |
1 | g.154571293T>A | CA342630096 | CHRNB2 | c.470T>A (p.Ile157Asn) c.476T>A (p.Ile159Asn) c.-9-32T>A (n.-9-32T>A) n.722T>A | ClinVar |
1 | g.154571293T>C | CA1130737 | CHRNB2 | c.470T>C (p.Ile157Thr) c.476T>C (p.Ile159Thr) c.-9-32T>C (n.-9-32T>C) n.722T>C | dbSNP ExAC gnomAD v4 |
1 | g.154571293T>G | CA342630097 | CHRNB2 | c.470T>G (p.Ile157Ser) c.476T>G (p.Ile159Ser) c.-9-32T>G (n.-9-32T>G) n.722T>G | |
1 | g.154571293T= | CA2480925210 | CHRNB2 | c.470T= (p.Ile157=) c.476T= (p.Ile159=) c.-9-32T= (n.-9-32T=) n.722T= | |
1 | g.154571294T>A | CA421230841 | CHRNB2 | c.471T>A (p.Ile157=) c.477T>A (p.Ile159=) c.-9-31T>A (n.-9-31T>A) n.723T>A | |
1 | g.154571294T>C | CA421230844 | CHRNB2 | c.471T>C (p.Ile157=) c.477T>C (p.Ile159=) c.-9-31T>C (n.-9-31T>C) n.723T>C | |
1 | g.154571294T>G | CA342630098 | CHRNB2 | c.471T>G (p.Ile157Met) c.477T>G (p.Ile159Met) c.-9-31T>G (n.-9-31T>G) n.723T>G | |
1 | g.154571295G>A | CA342630099 | CHRNB2 | c.472G>A (p.Glu158Lys) c.478G>A (p.Glu160Lys) c.-9-30G>A (n.-9-30G>A) n.724G>A | |
1 | g.154571295G>C | CA342630100 | CHRNB2 | c.472G>C (p.Glu158Gln) c.478G>C (p.Glu160Gln) c.-9-30G>C (n.-9-30G>C) n.724G>C | |
1 | g.154571295G>T | CA342630101 | CHRNB2 | c.472G>T (p.Glu158Ter) c.478G>T (p.Glu160Ter) c.-9-30G>T (n.-9-30G>T) n.724G>T | |
1 | g.154571296A>C | CA342630102 | CHRNB2 | c.473A>C (p.Glu158Ala) c.479A>C (p.Glu160Ala) c.-9-29A>C (n.-9-29A>C) n.725A>C | |
1 | g.154571296A>G | CA342630103 | CHRNB2 | c.473A>G (p.Glu158Gly) c.479A>G (p.Glu160Gly) c.-9-29A>G (n.-9-29A>G) n.725A>G | |
1 | g.154571296A>T | CA342630104 | CHRNB2 | c.473A>T (p.Glu158Val) c.479A>T (p.Glu160Val) c.-9-29A>T (n.-9-29A>T) n.725A>T | |
1 | g.154571297A>C | CA342630105 | CHRNB2 | c.474A>C (p.Glu158Asp) c.480A>C (p.Glu160Asp) c.-9-28A>C (n.-9-28A>C) n.726A>C | |
1 | g.154571297A>G | CA421230845 | CHRNB2 | c.474A>G (p.Glu158=) c.480A>G (p.Glu160=) c.-9-28A>G (n.-9-28A>G) n.726A>G | |
1 | g.154571297A>T | CA342630106 | CHRNB2 | c.474A>T (p.Glu158Asp) c.480A>T (p.Glu160Asp) c.-9-28A>T (n.-9-28A>T) n.726A>T | |
1 | g.154571298G>A | CA342630107 | CHRNB2 | c.475G>A (p.Val159Ile) c.481G>A (p.Val161Ile) c.-9-27G>A (n.-9-27G>A) n.727G>A | |
1 | g.154571298G>C | CA342630109 | CHRNB2 | c.475G>C (p.Val159Leu) c.481G>C (p.Val161Leu) c.-9-27G>C (n.-9-27G>C) n.727G>C | |
1 | g.154571298G>T | CA342630108 | CHRNB2 | c.475G>T (p.Val159Leu) c.481G>T (p.Val161Leu) c.-9-27G>T (n.-9-27G>T) n.727G>T | |
1 | g.154571299T>A | CA342630110 | CHRNB2 | c.476T>A (p.Val159Glu) c.482T>A (p.Val161Glu) c.-9-26T>A (n.-9-26T>A) n.728T>A | |
1 | g.154571299T>C | CA342630112 | CHRNB2 | c.476T>C (p.Val159Ala) c.482T>C (p.Val161Ala) c.-9-26T>C (n.-9-26T>C) n.728T>C | |
1 | g.154571299T>G | CA342630111 | CHRNB2 | c.476T>G (p.Val159Gly) c.482T>G (p.Val161Gly) c.-9-26T>G (n.-9-26T>G) n.728T>G | COSMIC |
1 | g.154571300A>C | CA421230850 | CHRNB2 | c.477A>C (p.Val159=) c.483A>C (p.Val161=) c.-9-25A>C (n.-9-25A>C) n.729A>C | |
1 | g.154571300A>G | CA421230849 | CHRNB2 | c.477A>G (p.Val159=) c.483A>G (p.Val161=) c.-9-25A>G (n.-9-25A>G) n.729A>G | |
1 | g.154571300A>T | CA421230848 | CHRNB2 | c.477A>T (p.Val159=) c.483A>T (p.Val161=) c.-9-25A>T (n.-9-25A>T) n.729A>T | |
1 | g.154571301A>C | CA342630113 | CHRNB2 | c.478A>C (p.Lys160Gln) c.484A>C (p.Lys162Gln) c.-9-24A>C (n.-9-24A>C) n.730A>C | |
1 | g.154571301A>G | CA342630114 | CHRNB2 | c.478A>G (p.Lys160Glu) c.484A>G (p.Lys162Glu) c.-9-24A>G (n.-9-24A>G) n.730A>G | |
1 | g.154571301A>T | CA342630115 | CHRNB2 | c.478A>T (p.Lys160Ter) c.484A>T (p.Lys162Ter) c.-9-24A>T (n.-9-24A>T) n.730A>T | |
1 | g.154571302A>C | CA342630116 | CHRNB2 | c.479A>C (p.Lys160Thr) c.485A>C (p.Lys162Thr) c.-9-23A>C (n.-9-23A>C) n.731A>C | |
1 | g.154571302A>G | CA342630117 | CHRNB2 | c.479A>G (p.Lys160Arg) c.485A>G (p.Lys162Arg) c.-9-23A>G (n.-9-23A>G) n.731A>G | |
1 | g.154571302A>T | CA342630118 | CHRNB2 | c.479A>T (p.Lys160Met) c.485A>T (p.Lys162Met) c.-9-23A>T (n.-9-23A>T) n.731A>T |