6 | g.49451603_49451604del | CA567155985 | MMUT | c.1196_1197del (p.Val399GlufsTer24)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.49451603C>A | CA364398915 | MMUT | c.1195G>T (p.Val399Leu)
| |
6 | g.49451603C>G | CA364398916 | MMUT | c.1195G>C (p.Val399Leu)
| |
6 | g.49451603C>T | CA364398917 | MMUT | c.1195G>A (p.Val399Met)
| gnomAD v4 |
6 | g.49451604A>C | CA450606520 | MMUT | c.1194T>G (p.Thr398=)
| |
6 | g.49451604A>G | CA450606521 | MMUT | c.1194T>C (p.Thr398=)
| |
6 | g.49451604A>T | CA450606522 | MMUT | c.1194T>A (p.Thr398=)
| |
6 | g.49451605G>A | CA364398918 | MMUT | c.1193C>T (p.Thr398Ile)
| gnomAD v4 |
6 | g.49451605G>C | CA364398919 | MMUT | c.1193C>G (p.Thr398Ser)
| |
6 | g.49451605G>T | CA364398920 | MMUT | c.1193C>A (p.Thr398Asn)
| |
6 | g.49451606T>A | CA364398921 | MMUT | c.1192A>T (p.Thr398Ser)
| |
6 | g.49451606T>C | CA364398922 | MMUT | c.1192A>G (p.Thr398Ala)
| gnomAD v4 COSMIC |
6 | g.49451606T>G | CA364398923 | MMUT | c.1192A>C (p.Thr398Pro)
| gnomAD v4 |
6 | g.49451607T>A | CA450606531 | MMUT | c.1191A>T (p.Pro397=)
| |
6 | g.49451607T>C | CA450606532 | MMUT | c.1191A>G (p.Pro397=)
| |
6 | g.49451607T>G | CA450606533 | MMUT | c.1191A>C (p.Pro397=)
| ClinVar dbSNP gnomAD v4 |
6 | g.49451608G>A | CA3846945 | MMUT | c.1190C>T (p.Pro397Leu)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49451608G>C | CA364398925 | MMUT | c.1190C>G (p.Pro397Arg)
| |
6 | g.49451608G= | CA1627389339 | MMUT | c.1190C= (p.Pro397=)
| |
6 | g.49451608G>T | CA364398924 | MMUT | c.1190C>A (p.Pro397Gln)
| |
6 | g.49451609del | CA2679046693 | MMUT | c.1190del (p.Pro397GlnfsTer3)
| gnomAD v4 |
6 | g.49451609G>A | CA364398926 | MMUT | c.1189C>T (p.Pro397Ser)
| |
6 | g.49451609G>C | CA364398927 | MMUT | c.1189C>G (p.Pro397Ala)
| |
6 | g.49451609G>T | CA364398928 | MMUT | c.1189C>A (p.Pro397Thr)
| |
6 | g.49451610C>A | CA364398929 | MMUT | c.1188G>T (p.Leu396Phe)
| |
6 | g.49451610C>G | CA364398930 | MMUT | c.1188G>C (p.Leu396Phe)
| |
6 | g.49451610C>T | CA450606541 | MMUT | c.1188G>A (p.Leu396=)
| |
6 | g.49451611A>C | CA364398931 | MMUT | c.1187T>G (p.Leu396Trp)
| |
6 | g.49451611A>G | CA364398932 | MMUT | c.1187T>C (p.Leu396Ser)
| |
6 | g.49451611A>T | CA364398933 | MMUT | c.1187T>A (p.Leu396Ter)
| |
6 | g.49451612A>C | CA364398934 | MMUT | c.1186T>G (p.Leu396Val)
| |
6 | g.49451612A>G | CA450606549 | MMUT | c.1186T>C (p.Leu396=)
| |
6 | g.49451612A>T | CA364398935 | MMUT | c.1186T>A (p.Leu396Met)
| gnomAD v4 |
6 | g.49451613A>C | CA450606552 | MMUT | c.1185T>G (p.Gly395=)
| |
6 | g.49451613A>G | CA450606554 | MMUT | c.1185T>C (p.Gly395=)
| |
6 | g.49451613A>T | CA450606555 | MMUT | c.1185T>A (p.Gly395=)
| gnomAD v4 |
6 | g.49451614C>A | CA364398936 | MMUT | c.1184G>T (p.Gly395Val)
| gnomAD v4 |
6 | g.49451614C= | CA1627389340 | MMUT | c.1184G= (p.Gly395=)
| |
6 | g.49451614C>G | CA364398937 | MMUT | c.1184G>C (p.Gly395Ala)
| |
6 | g.49451614C>T | CA3846946 | MMUT | c.1184G>A (p.Gly395Asp)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49451615C>A | CA364398940 | MMUT | c.1183G>T (p.Gly395Cys)
| |
6 | g.49451615C>G | CA364398938 | MMUT | c.1183G>C (p.Gly395Arg)
| |
6 | g.49451615C>T | CA364398939 | MMUT | c.1183G>A (p.Gly395Ser)
| |
6 | g.49451616C>A | CA364398941 | MMUT | c.1182G>T (p.Leu394Phe)
| |
6 | g.49451616C= | CA1627389341 | MMUT | c.1182G= (p.Leu394=)
| |
6 | g.49451616C>G | CA364398942 | MMUT | c.1182G>C (p.Leu394Phe)
| |
6 | g.49451616C>T | CA3846947 | MMUT | c.1182G>A (p.Leu394=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49451617A>C | CA364398943 | MMUT | c.1181T>G (p.Leu394Trp)
| |
6 | g.49451617A>G | CA364398944 | MMUT | c.1181T>C (p.Leu394Ser)
| |
6 | g.49451617A>T | CA364398945 | MMUT | c.1181T>A (p.Leu394Ter)
| |
6 | g.49451619dup | CA10575868 | MMUT | c.1181dup (p.Leu394PhefsTer30)
| ClinVar dbSNP gnomAD v4 |
6 | g.49451618A>C | CA364398946 | MMUT | c.1180T>G (p.Leu394Val)
| |
6 | g.49451618A>G | CA450606570 | MMUT | c.1180T>C (p.Leu394=)
| ClinVar dbSNP |
6 | g.49451618A>T | CA364398947 | MMUT | c.1180T>A (p.Leu394Met)
| |
6 | g.49451619A>C | CA450606577 | MMUT | c.1179T>G (p.Ala393=)
| |
6 | g.49451619A>G | CA450606574 | MMUT | c.1179T>C (p.Ala393=)
| |
6 | g.49451619A>T | CA450606575 | MMUT | c.1179T>A (p.Ala393=)
| |
6 | g.49451620G>A | CA364398948 | MMUT | c.1178C>T (p.Ala393Val)
| gnomAD v4 |
6 | g.49451620G>C | CA364398949 | MMUT | c.1178C>G (p.Ala393Gly)
| |
6 | g.49451620G>T | CA364398950 | MMUT | c.1178C>A (p.Ala393Asp)
| |
6 | g.49451621C>A | CA364398951 | MMUT | c.1177G>T (p.Ala393Ser)
| |
6 | g.49451621C>G | CA364398953 | MMUT | c.1177G>C (p.Ala393Pro)
| |
6 | g.49451621C>T | CA364398952 | MMUT | c.1177G>A (p.Ala393Thr)
| |
6 | g.49451622T>A | CA364398954 | MMUT | c.1176A>T (p.Glu392Asp)
| |
6 | g.49451622T>C | CA450606585 | MMUT | c.1176A>G (p.Glu392=)
| |
6 | g.49451622T>G | CA364398955 | MMUT | c.1176A>C (p.Glu392Asp)
| |
6 | g.49451623T>A | CA364398956 | MMUT | c.1175A>T (p.Glu392Val)
| |
6 | g.49451623T>C | CA364398957 | MMUT | c.1175A>G (p.Glu392Gly)
| |
6 | g.49451623T>G | CA364398958 | MMUT | c.1175A>C (p.Glu392Ala)
| |
6 | g.49451624C>A | CA364398959 | MMUT | c.1174G>T (p.Glu392Ter)
| COSMIC |
6 | g.49451624C>G | CA364398960 | MMUT | c.1174G>C (p.Glu392Gln)
| |
6 | g.49451624C>T | CA364398961 | MMUT | c.1174G>A (p.Glu392Lys)
| |
6 | g.49451625A>C | CA364398962 | MMUT | c.1173T>G (p.Asp391Glu)
| |
6 | g.49451625A>G | CA450606595 | MMUT | c.1173T>C (p.Asp391=)
| |
6 | g.49451625A>T | CA364398963 | MMUT | c.1173T>A (p.Asp391Glu)
| gnomAD v4 |
6 | g.49451626T>A | CA364398964 | MMUT | c.1172A>T (p.Asp391Val)
| |
6 | g.49451626T>C | CA364398965 | MMUT | c.1172A>G (p.Asp391Gly)
| |
6 | g.49451626T>G | CA364398966 | MMUT | c.1172A>C (p.Asp391Ala)
| |
6 | g.49451626_49451627delinsA | CA2580074726 | MMUT | c.1171_1172delinsT (p.Asp391LeufsTer9)
| ClinVar |
6 | g.49451627C>A | CA364398967 | MMUT | c.1171G>T (p.Asp391Tyr)
| |
6 | g.49451627C>G | CA364398968 | MMUT | c.1171G>C (p.Asp391His)
| |
6 | g.49451627C>T | CA364398969 | MMUT | c.1171G>A (p.Asp391Asn)
| gnomAD v4 |
6 | g.49451628A= | CA1627389342 | MMUT | c.1170T= (p.Phe390=)
| |
6 | g.49451628A>C | CA364398970 | MMUT | c.1170T>G (p.Phe390Leu)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.49451628A>G | CA450606603 | MMUT | c.1170T>C (p.Phe390=)
| |
6 | g.49451628A>T | CA364398971 | MMUT | c.1170T>A (p.Phe390Leu)
| |
6 | g.49451629A>C | CA364398972 | MMUT | c.1169T>G (p.Phe390Cys)
| |
6 | g.49451629A>G | CA364398973 | MMUT | c.1169T>C (p.Phe390Ser)
| gnomAD v4 |
6 | g.49451629A>T | CA364398974 | MMUT | c.1169T>A (p.Phe390Tyr)
| |
6 | g.49451630A>C | CA364398975 | MMUT | c.1168T>G (p.Phe390Val)
| |
6 | g.49451630A>G | CA364398976 | MMUT | c.1168T>C (p.Phe390Leu)
| |
6 | g.49451630A>T | CA364398977 | MMUT | c.1168T>A (p.Phe390Ile)
| |
6 | g.49451632_49451634del | CA2679046694 | MMUT | c.1166_1168del (p.Ser389del)
| gnomAD v4 |
6 | g.49451631A= | CA1627389343 | MMUT | c.1167T= (p.Ser389=)
| |
6 | g.49451631A>C | CA450606611 | MMUT | c.1167T>G (p.Ser389=)
| |
6 | g.49451631A>G | CA450606612 | MMUT | c.1167T>C (p.Ser389=)
| |
6 | g.49451631A>T | CA450606613 | MMUT | c.1167T>A (p.Ser389=)
| dbSNP |
6 | g.49451632G>A | CA364398978 | MMUT | c.1166C>T (p.Ser389Phe)
| |
6 | g.49451632G>C | CA364398979 | MMUT | c.1166C>G (p.Ser389Cys)
| gnomAD v4 |
6 | g.49451632G>T | CA364398980 | MMUT | c.1166C>A (p.Ser389Tyr)
| |
6 | g.49451633A= | CA1627389344 | MMUT | c.1165T= (p.Ser389=)
| |
6 | g.49451633A>C | CA364398981 | MMUT | c.1165T>G (p.Ser389Ala)
| |
6 | g.49451633A>G | CA364398982 | MMUT | c.1165T>C (p.Ser389Pro)
| dbSNP |
6 | g.49451633A>T | CA364398983 | MMUT | c.1165T>A (p.Ser389Thr)
| |
6 | g.49451634A= | CA1627389345 | MMUT | c.1164T= (p.Asn388=)
| |
6 | g.49451634A>C | CA364398984 | MMUT | c.1164T>G (p.Asn388Lys)
| |
6 | g.49451634A>G | CA450606614 | MMUT | c.1164T>C (p.Asn388=)
| ClinVar dbSNP gnomAD v4 |
6 | g.49451634A>T | CA10575869 | MMUT | c.1164T>A (p.Asn388Lys)
| ClinVar dbSNP |
6 | g.49451635T>A | CA364398985 | MMUT | c.1163A>T (p.Asn388Ile)
| |
6 | g.49451635T>C | CA364398986 | MMUT | c.1163A>G (p.Asn388Ser)
| gnomAD v4 |
6 | g.49451635T>G | CA364398987 | MMUT | c.1163A>C (p.Asn388Thr)
| |
6 | g.49451636T>A | CA364398988 | MMUT | c.1162A>T (p.Asn388Tyr)
| |
6 | g.49451636T>C | CA3846948 | MMUT | c.1162A>G (p.Asn388Asp)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49451636T>G | CA364398989 | MMUT | c.1162A>C (p.Asn388His)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.49451636T= | CA1627389346 | MMUT | c.1162A= (p.Asn388=)
| |
6 | g.49451637T>A | CA450606615 | MMUT | c.1161A>T (p.Thr387=)
| |
6 | g.49451637T>C | CA450606617 | MMUT | c.1161A>G (p.Thr387=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
6 | g.49451637T>G | CA450606616 | MMUT | c.1161A>C (p.Thr387=)
| |
6 | g.49451637T= | CA1627389347 | MMUT | c.1161A= (p.Thr387=)
| |
6 | g.49451641_49451642del | CA2578717902 | MMUT | c.1160_1161del (p.Thr387LysfsTer4)
| |
6 | g.49451638G>A | CA364398992 | MMUT | c.1160C>T (p.Thr387Ile)
| ClinVar dbSNP |
6 | g.49451638G>C | CA364398990 | MMUT | c.1160C>G (p.Thr387Arg)
| |
6 | g.49451638G= | CA1627389348 | MMUT | c.1160C= (p.Thr387=)
| |
6 | g.49451638G>T | CA364398991 | MMUT | c.1160C>A (p.Thr387Lys)
| ClinVar dbSNP gnomAD v4 |
6 | g.49451639T>A | CA364398993 | MMUT | c.1159A>T (p.Thr387Ser)
| |
6 | g.49451639T>C | CA364398994 | MMUT | c.1159A>G (p.Thr387Ala)
| |
6 | g.49451639T>G | CA364398995 | MMUT | c.1159A>C (p.Thr387Pro)
| ClinVar dbSNP gnomAD v4 |
6 | g.49451639T= | CA1627389349 | MMUT | c.1159A= (p.Thr387=)
| |
6 | g.49451640G>A | CA450606618 | MMUT | c.1158C>T (p.His386=)
| |
6 | g.49451640G>C | CA364398996 | MMUT | c.1158C>G (p.His386Gln)
| |
6 | g.49451640G>T | CA364398997 | MMUT | c.1158C>A (p.His386Gln)
| COSMIC |
6 | g.49451641T>A | CA364398998 | MMUT | c.1157A>T (p.His386Leu)
| |
6 | g.49451641T>C | CA138796375 | MMUT | c.1157A>G (p.His386Arg)
| dbSNP gnomAD v2 gnomAD v4 |
6 | g.49451641T>G | CA364398999 | MMUT | c.1157A>C (p.His386Pro)
| ClinVar |
6 | g.49451641T= | CA1627389350 | MMUT | c.1157A= (p.His386=)
| |
6 | g.49451642G>A | CA364399000 | MMUT | c.1156C>T (p.His386Tyr)
| |
6 | g.49451642G>C | CA364399001 | MMUT | c.1156C>G (p.His386Asp)
| |
6 | g.49451642G= | CA1627389351 | MMUT | c.1156C= (p.His386=)
| |
6 | g.49451642G>T | CA364399002 | MMUT | c.1156C>A (p.His386Asn)
| ClinVar dbSNP gnomAD v4 |
6 | g.49451643C>A | CA364399003 | MMUT | c.1155G>T (p.Leu385Phe)
| |
6 | g.49451643C>G | CA364399004 | MMUT | c.1155G>C (p.Leu385Phe)
| gnomAD v4 |
6 | g.49451643C>T | CA450606619 | MMUT | c.1155G>A (p.Leu385=)
| ClinVar dbSNP |
6 | g.49451644A>C | CA364399005 | MMUT | c.1154T>G (p.Leu385Trp)
| gnomAD v4 |
6 | g.49451644A>G | CA364399006 | MMUT | c.1154T>C (p.Leu385Ser)
| gnomAD v4 |
6 | g.49451644A>T | CA364399007 | MMUT | c.1154T>A (p.Leu385Ter)
| |
6 | g.49451646del | CA2679046696 | MMUT | c.1154del (p.Leu385CysfsTer15)
| gnomAD v4 |
6 | g.49451645_49451646del | CA2695206528 | MMUT | c.1153_1154del (p.Leu385AlafsTer6)
| |
6 | g.49451645A>C | CA364399008 | MMUT | c.1153T>G (p.Leu385Val)
| |
6 | g.49451645A>G | CA450606621 | MMUT | c.1153T>C (p.Leu385=)
| |
6 | g.49451645A>T | CA364399009 | MMUT | c.1153T>A (p.Leu385Met)
| |
6 | g.49451646A>C | CA450606622 | MMUT | c.1152T>G (p.Ser384=)
| ClinVar dbSNP |
6 | g.49451646A>G | CA450606623 | MMUT | c.1152T>C (p.Ser384=)
| |
6 | g.49451646A>T | CA450606624 | MMUT | c.1152T>A (p.Ser384=)
| |
6 | g.49451647G>A | CA364399012 | MMUT | c.1151C>T (p.Ser384Phe)
| dbSNP |
6 | g.49451647G>C | CA364399011 | MMUT | c.1151C>G (p.Ser384Cys)
| |
6 | g.49451647G= | CA1627389352 | MMUT | c.1151C= (p.Ser384=)
| |
6 | g.49451647G>T | CA364399010 | MMUT | c.1151C>A (p.Ser384Tyr)
| |
6 | g.49451648A>C | CA364399013 | MMUT | c.1150T>G (p.Ser384Ala)
| |
6 | g.49451648A>G | CA364399015 | MMUT | c.1150T>C (p.Ser384Pro)
| |
6 | g.49451648A>T | CA364399014 | MMUT | c.1150T>A (p.Ser384Thr)
| |
6 | g.49451649C>A | CA364399016 | MMUT | c.1149G>T (p.Gln383His)
| |
6 | g.49451649C= | CA1627389353 | MMUT | c.1149G= (p.Gln383=)
| |
6 | g.49451649C>G | CA364399017 | MMUT | c.1149G>C (p.Gln383His)
| |
6 | g.49451649C>T | CA450606626 | MMUT | c.1149G>A (p.Gln383=)
| |
6 | g.49451650T>A | CA364399018 | MMUT | c.1148A>T (p.Gln383Leu)
| |
6 | g.49451650T>C | CA364399019 | MMUT | c.1148A>G (p.Gln383Arg)
| dbSNP COSMIC |
6 | g.49451650T>G | CA364399020 | MMUT | c.1148A>C (p.Gln383Pro)
| |
6 | g.49451650T= | CA1627389354 | MMUT | c.1148A= (p.Gln383=)
| |
6 | g.49451650dup | CA3846949 | MMUT | c.1148dup (p.Ser384ValfsTer8)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49451650_49451651del | CA2573140874 | MMUT | c.1147_1148del (p.Gln383ValfsTer8)
| ClinVar dbSNP |
6 | g.49451651G>A | CA364399021 | MMUT | c.1147C>T (p.Gln383Ter)
| COSMIC |
6 | g.49451651G>C | CA364399022 | MMUT | c.1147C>G (p.Gln383Glu)
| |
6 | g.49451651G>T | CA364399023 | MMUT | c.1147C>A (p.Gln383Lys)
| |
6 | g.49451652A>C | CA450606628 | MMUT | c.1146T>G (p.Thr382=)
| |
6 | g.49451652A>G | CA450606630 | MMUT | c.1146T>C (p.Thr382=)
| |
6 | g.49451652A>T | CA450606629 | MMUT | c.1146T>A (p.Thr382=)
| ClinVar dbSNP gnomAD v4 |
6 | g.49451653G>A | CA364399024 | MMUT | c.1145C>T (p.Thr382Ile)
| |
6 | g.49451653G>C | CA364399025 | MMUT | c.1145C>G (p.Thr382Ser)
| |
6 | g.49451653G>T | CA364399026 | MMUT | c.1145C>A (p.Thr382Asn)
| |
6 | g.49451654T>A | CA364399027 | MMUT | c.1144A>T (p.Thr382Ser)
| |
6 | g.49451654T>C | CA364399028 | MMUT | c.1144A>G (p.Thr382Ala)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.49451654T>G | CA364399029 | MMUT | c.1144A>C (p.Thr382Pro)
| |
6 | g.49451654T= | CA1627389355 | MMUT | c.1144A= (p.Thr382=)
| |
6 | g.49451655C>A | CA450606631 | MMUT | c.1143G>T (p.Gly381=)
| |
6 | g.49451655C= | CA1627389356 | MMUT | c.1143G= (p.Gly381=)
| |
6 | g.49451655C>G | CA450606632 | MMUT | c.1143G>C (p.Gly381=)
| |
6 | g.49451655C>T | CA450606633 | MMUT | c.1143G>A (p.Gly381=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
6 | g.49451657del | CA2679046697 | MMUT | c.1143del (p.Thr382LeufsTer18)
| gnomAD v4 |
6 | g.49451656C>A | CA364399032 | MMUT | c.1142G>T (p.Gly381Val)
| ClinVar dbSNP |
6 | g.49451656C= | CA1627389357 | MMUT | c.1142G= (p.Gly381=)
| |
6 | g.49451656C>G | CA364399031 | MMUT | c.1142G>C (p.Gly381Ala)
| |
6 | g.49451656C>T | CA364399030 | MMUT | c.1142G>A (p.Gly381Glu)
| |
6 | g.49451657C>A | CA364399033 | MMUT | c.1141G>T (p.Gly381Trp)
| |
6 | g.49451657C>G | CA364399034 | MMUT | c.1141G>C (p.Gly381Arg)
| |
6 | g.49451657C>T | CA364399035 | MMUT | c.1141G>A (p.Gly381Arg)
| ClinVar gnomAD v4 |
6 | g.49451658T>A | CA450606635 | MMUT | c.1140A>T (p.Gly380=)
| |
6 | g.49451658T>C | CA450606634 | MMUT | c.1140A>G (p.Gly380=)
| |
6 | g.49451658T>G | CA450606636 | MMUT | c.1140A>C (p.Gly380=)
| |
6 | g.49451659C>A | CA364399036 | MMUT | c.1139G>T (p.Gly380Val)
| |
6 | g.49451659C= | CA1627389358 | MMUT | c.1139G= (p.Gly380=)
| |
6 | g.49451659C>G | CA364399037 | MMUT | c.1139G>C (p.Gly380Ala)
| |
6 | g.49451659C>T | CA3846950 | MMUT | c.1139G>A (p.Gly380Glu)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49451660C>A | CA364399038 | MMUT | c.1138G>T (p.Gly380Ter)
| |
6 | g.49451660C>G | CA364399039 | MMUT | c.1138G>C (p.Gly380Arg)
| |
6 | g.49451660C>T | CA364399040 | MMUT | c.1138G>A (p.Gly380Arg)
| |
6 | g.49451661A>C | CA364399041 | MMUT | c.1137T>G (p.Phe379Leu)
| |
6 | g.49451661A>G | CA450606637 | MMUT | c.1137T>C (p.Phe379=)
| |
6 | g.49451661A>T | CA364399042 | MMUT | c.1137T>A (p.Phe379Leu)
| |
6 | g.49451663del | CA2695206529 | MMUT | c.1137del (p.Phe379LeufsTer21)
| |
6 | g.49451662A= | CA1627389359 | MMUT | c.1136T= (p.Phe379=)
| |
6 | g.49451662A>C | CA3846951 | MMUT | c.1136T>G (p.Phe379Cys)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49451662A>G | CA364399043 | MMUT | c.1136T>C (p.Phe379Ser)
| |
6 | g.49451662A>T | CA364399044 | MMUT | c.1136T>A (p.Phe379Tyr)
| |
6 | g.49451663A>C | CA364399047 | MMUT | c.1135T>G (p.Phe379Val)
| |
6 | g.49451663A>G | CA364399046 | MMUT | c.1135T>C (p.Phe379Leu)
| |
6 | g.49451663A>T | CA364399045 | MMUT | c.1135T>A (p.Phe379Ile)
| |
6 | g.49451664T>A | CA450606639 | MMUT | c.1134A>T (p.Val378=)
| |
6 | g.49451664T>C | CA3846952 | MMUT | c.1134A>G (p.Val378=)
| dbSNP ExAC gnomAD v2 |
6 | g.49451664T>G | CA450606640 | MMUT | c.1134A>C (p.Val378=)
| |
6 | g.49451664T= | CA1627389360 | MMUT | c.1134A= (p.Val378=)
| |
6 | g.49451665A>C | CA364399048 | MMUT | c.1133T>G (p.Val378Gly)
| |
6 | g.49451665A>G | CA364399049 | MMUT | c.1133T>C (p.Val378Ala)
| |
6 | g.49451665A>T | CA364399050 | MMUT | c.1133T>A (p.Val378Glu)
| |
6 | g.49451666C>A | CA364399051 | MMUT | c.1132G>T (p.Val378Leu)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451666C= | CA1627389361 | MMUT | c.1132G= (p.Val378=)
| |
6 | g.49451666C>G | CA364399052 | MMUT | c.1132G>C (p.Val378Leu)
| |
6 | g.49451666C>T | CA364399053 | MMUT | c.1132G>A (p.Val378Ile)
| dbSNP gnomAD v2 gnomAD v4 |
6 | g.49451670_49451672del | CA2770993687 | MMUT | c.1130_1132del (p.Ala377del)
| |
6 | g.49451667T>A | CA450606641 | MMUT | c.1131A>T (p.Ala377=)
| |
6 | g.49451667T>C | CA450606642 | MMUT | c.1131A>G (p.Ala377=)
| ClinVar dbSNP |
6 | g.49451667T>G | CA450606643 | MMUT | c.1131A>C (p.Ala377=)
| |
6 | g.49451668G>A | CA364399054 | MMUT | c.1130C>T (p.Ala377Val)
| |
6 | g.49451668G>C | CA364399055 | MMUT | c.1130C>G (p.Ala377Gly)
| |
6 | g.49451668G= | CA1627389362 | MMUT | c.1130C= (p.Ala377=)
| |
6 | g.49451668G>T | CA115263 | MMUT | c.1130C>A (p.Ala377Glu)
| ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
6 | g.49451669C>A | CA364399056 | MMUT | c.1129G>T (p.Ala377Ser)
| |
6 | g.49451669C>G | CA364399057 | MMUT | c.1129G>C (p.Ala377Pro)
| |
6 | g.49451669C>T | CA364399058 | MMUT | c.1129G>A (p.Ala377Thr)
| gnomAD v4 |
6 | g.49451670T>A | CA450606644 | MMUT | c.1128A>T (p.Ala376=)
| |
6 | g.49451670T>C | CA450606645 | MMUT | c.1128A>G (p.Ala376=)
| gnomAD v4 |
6 | g.49451670T>G | CA450606646 | MMUT | c.1128A>C (p.Ala376=)
| |
6 | g.49451670_49451672delinsTGC | CA1627389363 | MMUT | c.1126_1128delinsGCA (p.Ala376=)
| |
6 | g.49451671G>A | CA364399061 | MMUT | c.1127C>T (p.Ala376Val)
| |
6 | g.49451671G>C | CA364399059 | MMUT | c.1127C>G (p.Ala376Gly)
| |
6 | g.49451671G>T | CA364399060 | MMUT | c.1127C>A (p.Ala376Glu)
| |
6 | g.49451671_49451672del | CA658683443 | MMUT | c.1126_1127del (p.Ala376SerfsTer15)
| ClinVar dbSNP gnomAD v4 |
6 | g.49451672C>A | CA364399062 | MMUT | c.1126G>T (p.Ala376Ser)
| |
6 | g.49451672C= | CA1627389364 | MMUT | c.1126G= (p.Ala376=)
| |
6 | g.49451672C>G | CA364399063 | MMUT | c.1126G>C (p.Ala376Pro)
| |
6 | g.49451672C>T | CA364399064 | MMUT | c.1126G>A (p.Ala376Thr)
| dbSNP gnomAD v2 gnomAD v4 |
6 | g.49451673C>A | CA364399065 | MMUT | c.1125G>T (p.Met375Ile)
| |
6 | g.49451673C= | CA1627389365 | MMUT | c.1125G= (p.Met375=)
| |
6 | g.49451673C>G | CA364399066 | MMUT | c.1125G>C (p.Met375Ile)
| |
6 | g.49451673C>T | CA3846953 | MMUT | c.1125G>A (p.Met375Ile)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451674A>C | CA364399067 | MMUT | c.1124T>G (p.Met375Arg)
| |
6 | g.49451674A>G | CA364399068 | MMUT | c.1124T>C (p.Met375Thr)
| gnomAD v3 gnomAD v4 |
6 | g.49451674A>T | CA364399069 | MMUT | c.1124T>A (p.Met375Lys)
| |
6 | g.49451675T>A | CA364399070 | MMUT | c.1123A>T (p.Met375Leu)
| |
6 | g.49451675T>C | CA364399071 | MMUT | c.1123A>G (p.Met375Val)
| gnomAD v4 |
6 | g.49451675T>G | CA364399072 | MMUT | c.1123A>C (p.Met375Leu)
| |
6 | g.49451676T>A | CA450606647 | MMUT | c.1122A>T (p.Ala374=)
| |
6 | g.49451676T>C | CA450606648 | MMUT | c.1122A>G (p.Ala374=)
| |
6 | g.49451676T>G | CA450606649 | MMUT | c.1122A>C (p.Ala374=)
| |
6 | g.49451677G>A | CA364399075 | MMUT | c.1121C>T (p.Ala374Val)
| |
6 | g.49451677G>C | CA364399073 | MMUT | c.1121C>G (p.Ala374Gly)
| |
6 | g.49451677G>T | CA364399074 | MMUT | c.1121C>A (p.Ala374Glu)
| |
6 | g.49451678C>A | CA364399076 | MMUT | c.1120G>T (p.Ala374Ser)
| |
6 | g.49451678C>G | CA364399078 | MMUT | c.1120G>C (p.Ala374Pro)
| |
6 | g.49451678C>T | CA364399077 | MMUT | c.1120G>A (p.Ala374Thr)
| gnomAD v4 |
6 | g.49451679T>A | CA364399079 | MMUT | c.1119A>T (p.Glu373Asp)
| |
6 | g.49451679T>C | CA3846954 | MMUT | c.1119A>G (p.Glu373=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49451679T>G | CA364399080 | MMUT | c.1119A>C (p.Glu373Asp)
| |
6 | g.49451679T= | CA1627389366 | MMUT | c.1119A= (p.Glu373=)
| |
6 | g.49451680T>A | CA364399081 | MMUT | c.1118A>T (p.Glu373Val)
| |
6 | g.49451680T>C | CA364399082 | MMUT | c.1118A>G (p.Glu373Gly)
| ClinVar dbSNP |
6 | g.49451680T>G | CA364399084 | MMUT | c.1118A>C (p.Glu373Ala)
| |
6 | g.49451681C>A | CA364399086 | MMUT | c.1117G>T (p.Glu373Ter)
| COSMIC |
6 | g.49451681C>G | CA364399088 | MMUT | c.1117G>C (p.Glu373Gln)
| |
6 | g.49451681C>T | CA364399090 | MMUT | c.1117G>A (p.Glu373Lys)
| |
6 | g.49451682T>A | CA450606651 | MMUT | c.1116A>T (p.Ile372=)
| |
6 | g.49451682T>C | CA3846955 | MMUT | c.1116A>G (p.Ile372Met)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49451682T>G | CA450606650 | MMUT | c.1116A>C (p.Ile372=)
| |
6 | g.49451682T= | CA1627389367 | MMUT | c.1116A= (p.Ile372=)
| |
6 | g.49451683A= | CA1627389368 | MMUT | c.1115T= (p.Ile372=)
| |
6 | g.49451683A>C | CA364399096 | MMUT | c.1115T>G (p.Ile372Arg)
| |
6 | g.49451683A>G | CA3846956 | MMUT | c.1115T>C (p.Ile372Thr)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451683A>T | CA364399093 | MMUT | c.1115T>A (p.Ile372Lys)
| |
6 | g.49451683_49451706del | CA913110642 | MMUT | c.1092_1115del (p.Tyr364Ter)
| |
6 | g.49451683_49451706delinsATTGCAGTACGGACAATATTATTG | CA1627389369 | MMUT | c.1092_1115delinsCAATAATATTGTCCGTACTGCAAT (p.Tyr364=)
| |
6 | g.49451684T>A | CA364399098 | MMUT | c.1114A>T (p.Ile372Leu)
| |
6 | g.49451684T>C | CA3846957 | MMUT | c.1114A>G (p.Ile372Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49451684T>G | CA364399101 | MMUT | c.1114A>C (p.Ile372Leu)
| |
6 | g.49451684T= | CA1627389370 | MMUT | c.1114A= (p.Ile372=)
| |
6 | g.49451685_49451707del | CA567155986 | MMUT | c.1092_1114del (p.Asn365ArgfsTer19)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451685T>A | CA450606652 | MMUT | c.1113A>T (p.Ala371=)
| |
6 | g.49451685T>C | CA450606654 | MMUT | c.1113A>G (p.Ala371=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
6 | g.49451685T>G | CA450606653 | MMUT | c.1113A>C (p.Ala371=)
| ClinVar dbSNP gnomAD v4 |
6 | g.49451685T= | CA1627389371 | MMUT | c.1113A= (p.Ala371=)
| |
6 | g.49451686G>A | CA364399106 | MMUT | c.1112C>T (p.Ala371Val)
| ClinVar |
6 | g.49451686G>C | CA364399108 | MMUT | c.1112C>G (p.Ala371Gly)
| |
6 | g.49451686G>T | CA364399109 | MMUT | c.1112C>A (p.Ala371Glu)
| |
6 | g.49451687C>A | CA364399111 | MMUT | c.1111G>T (p.Ala371Ser)
| |
6 | g.49451687C>G | CA364399113 | MMUT | c.1111G>C (p.Ala371Pro)
| |
6 | g.49451687C>T | CA364399115 | MMUT | c.1111G>A (p.Ala371Thr)
| gnomAD v4 |
6 | g.49451688A>C | CA450606655 | MMUT | c.1110T>G (p.Thr370=)
| |
6 | g.49451688A>G | CA450606656 | MMUT | c.1110T>C (p.Thr370=)
| dbSNP gnomAD v4 |
6 | g.49451688A>T | CA450606657 | MMUT | c.1110T>A (p.Thr370=)
| |
6 | g.49451689G>A | CA364399118 | MMUT | c.1109C>T (p.Thr370Ile)
| |
6 | g.49451689G>C | CA364399120 | MMUT | c.1109C>G (p.Thr370Ser)
| |
6 | g.49451689G>T | CA364399122 | MMUT | c.1109C>A (p.Thr370Asn)
| |
6 | g.49451690T>A | CA364399127 | MMUT | c.1108A>T (p.Thr370Ser)
| |
6 | g.49451690T>C | CA364399125 | MMUT | c.1108A>G (p.Thr370Ala)
| ClinVar gnomAD v4 |
6 | g.49451690T>G | CA312765 | MMUT | c.1108A>C (p.Thr370Pro)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451690T= | CA1627389372 | MMUT | c.1108A= (p.Thr370=)
| |
6 | g.49451691A>C | CA450606658 | MMUT | c.1107T>G (p.Arg369=)
| |
6 | g.49451691A>G | CA450606659 | MMUT | c.1107T>C (p.Arg369=)
| gnomAD v4 COSMIC |
6 | g.49451691A>T | CA450606660 | MMUT | c.1107T>A (p.Arg369=)
| |
6 | g.49451691dup | CA1139659593 | MMUT | c.1107dup (p.Thr370TyrfsTer22)
| ClinVar dbSNP |
6 | g.49451692C>A | CA364399132 | MMUT | c.1106G>T (p.Arg369Leu)
| COSMIC |
6 | g.49451692C= | CA1627389373 | MMUT | c.1106G= (p.Arg369=)
| |
6 | g.49451692C>G | CA364399129 | MMUT | c.1106G>C (p.Arg369Pro)
| COSMIC |
6 | g.49451692C>T | CA312764 | MMUT | c.1106G>A (p.Arg369His)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
6 | g.49451693G>A | CA347895 | MMUT | c.1105C>T (p.Arg369Cys)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451693G>C | CA364399134 | MMUT | c.1105C>G (p.Arg369Gly)
| |
6 | g.49451693G= | CA1627389374 | MMUT | c.1105C= (p.Arg369=)
| |
6 | g.49451693G>T | CA364399136 | MMUT | c.1105C>A (p.Arg369Ser)
| |
6 | g.49451694G>A | CA450606661 | MMUT | c.1104C>T (p.Val368=)
| |
6 | g.49451694G>C | CA450606662 | MMUT | c.1104C>G (p.Val368=)
| |
6 | g.49451694G>T | CA450606663 | MMUT | c.1104C>A (p.Val368=)
| |
6 | g.49451695A>C | CA364399139 | MMUT | c.1103T>G (p.Val368Gly)
| |
6 | g.49451695A>G | CA364399140 | MMUT | c.1103T>C (p.Val368Ala)
| gnomAD v4 |
6 | g.49451695A>T | CA364399141 | MMUT | c.1103T>A (p.Val368Asp)
| |
6 | g.49451695_49451696delinsAC | CA1627389375 | MMUT | c.1102_1103delinsGT (p.Val368=)
| |
6 | g.49451696del | CA1139659594 | MMUT | c.1102del (p.Val368SerfsTer5)
| ClinVar dbSNP |
6 | g.49451696C>A | CA364399142 | MMUT | c.1102G>T (p.Val368Phe)
| |
6 | g.49451696C= | CA1627389376 | MMUT | c.1102G= (p.Val368=)
| |
6 | g.49451696C>G | CA364399144 | MMUT | c.1102G>C (p.Val368Leu)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451696C>T | CA364399145 | MMUT | c.1102G>A (p.Val368Ile)
| |
6 | g.49451697A= | CA1627389377 | MMUT | c.1101T= (p.Ile367=)
| |
6 | g.49451697A>C | CA364399146 | MMUT | c.1101T>G (p.Ile367Met)
| |
6 | g.49451697A>G | CA450606664 | MMUT | c.1101T>C (p.Ile367=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.49451697A>T | CA450606665 | MMUT | c.1101T>A (p.Ile367=)
| |
6 | g.49451698A>C | CA364399152 | MMUT | c.1100T>G (p.Ile367Ser)
| |
6 | g.49451698A>G | CA364399151 | MMUT | c.1100T>C (p.Ile367Thr)
| gnomAD v4 |
6 | g.49451698A>T | CA364399149 | MMUT | c.1100T>A (p.Ile367Asn)
| |
6 | g.49451699T>A | CA364399153 | MMUT | c.1099A>T (p.Ile367Phe)
| |
6 | g.49451699T>C | CA364399154 | MMUT | c.1099A>G (p.Ile367Val)
| |
6 | g.49451699T>G | CA364399155 | MMUT | c.1099A>C (p.Ile367Leu)
| |
6 | g.49451700A= | CA1627389378 | MMUT | c.1098T= (p.Asn366=)
| |
6 | g.49451700A>C | CA364399156 | MMUT | c.1098T>G (p.Asn366Lys)
| |
6 | g.49451700A>G | CA450606666 | MMUT | c.1098T>C (p.Asn366=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49451700A>T | CA364399159 | MMUT | c.1098T>A (p.Asn366Lys)
| |
6 | g.49451701T>A | CA364399161 | MMUT | c.1097A>T (p.Asn366Ile)
| |
6 | g.49451701T>C | CA347901 | MMUT | c.1097A>G (p.Asn366Ser)
| ClinVar dbSNP |
6 | g.49451701T>G | CA364399163 | MMUT | c.1097A>C (p.Asn366Thr)
| |
6 | g.49451701T= | CA1627389379 | MMUT | c.1097A= (p.Asn366=)
| |
6 | g.49451702T>A | CA364399165 | MMUT | c.1096A>T (p.Asn366Tyr)
| |
6 | g.49451702T>C | CA364399166 | MMUT | c.1096A>G (p.Asn366Asp)
| |
6 | g.49451702T>G | CA364399167 | MMUT | c.1096A>C (p.Asn366His)
| |
6 | g.49451703A>C | CA364399169 | MMUT | c.1095T>G (p.Asn365Lys)
| |
6 | g.49451703A>G | CA450606667 | MMUT | c.1095T>C (p.Asn365=)
| |
6 | g.49451703A>T | CA364399171 | MMUT | c.1095T>A (p.Asn365Lys)
| |