Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.16132140T>A | CA338622373 | EPHA2 | c.2249A>T (p.Asn750Ile) c.2087A>T (p.Asn696Ile) | |
1 | g.16132140T>C | CA338622374 | EPHA2 | c.2249A>G (p.Asn750Ser) c.2087A>G (p.Asn696Ser) | gnomAD v4 |
1 | g.16132140T>G | CA338622375 | EPHA2 | c.2249A>C (p.Asn750Thr) c.2087A>C (p.Asn696Thr) | |
1 | g.16132141T>A | CA338622376 | EPHA2 | c.2248A>T (p.Asn750Tyr) c.2086A>T (p.Asn696Tyr) | |
1 | g.16132141T>C | CA338622377 | EPHA2 | c.2248A>G (p.Asn750Asp) c.2086A>G (p.Asn696Asp) | gnomAD v4 |
1 | g.16132141T>G | CA338622378 | EPHA2 | c.2248A>C (p.Asn750His) c.2086A>C (p.Asn696His) | |
1 | g.16132142G>A | CA416385550 | EPHA2 | c.2247C>T (p.Ser749=) c.2085C>T (p.Ser695=) | |
1 | g.16132142G>C | CA338622379 | EPHA2 | c.2247C>G (p.Ser749Arg) c.2085C>G (p.Ser695Arg) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.16132142G= | CA1155650058 | EPHA2 | c.2247C= (p.Ser749=) c.2085C= (p.Ser695=) | |
1 | g.16132142G>T | CA338622380 | EPHA2 | c.2247C>A (p.Ser749Arg) c.2085C>A (p.Ser695Arg) | |
1 | g.16132143C>A | CA338622383 | EPHA2 | c.2246G>T (p.Ser749Ile) c.2084G>T (p.Ser695Ile) | |
1 | g.16132143C= | CA1155650061 | EPHA2 | c.2246G= (p.Ser749=) c.2084G= (p.Ser695=) | |
1 | g.16132143C>G | CA338622382 | EPHA2 | c.2246G>C (p.Ser749Thr) c.2084G>C (p.Ser695Thr) | |
1 | g.16132143C>T | CA338622381 | EPHA2 | c.2246G>A (p.Ser749Asn) c.2084G>A (p.Ser695Asn) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
1 | g.16132144T>A | CA338622384 | EPHA2 | c.2245A>T (p.Ser749Cys) c.2083A>T (p.Ser695Cys) | |
1 | g.16132144T>C | CA338622385 | EPHA2 | c.2245A>G (p.Ser749Gly) c.2083A>G (p.Ser695Gly) | dbSNP |
1 | g.16132144T>G | CA338622386 | EPHA2 | c.2245A>C (p.Ser749Arg) c.2083A>C (p.Ser695Arg) | |
1 | g.16132145G>A | CA416385551 | EPHA2 | c.2244C>T (p.Asn748=) c.2082C>T (p.Asn694=) | dbSNP gnomAD v4 |
1 | g.16132145G>C | CA338622387 | EPHA2 | c.2244C>G (p.Asn748Lys) c.2082C>G (p.Asn694Lys) | |
1 | g.16132145G>T | CA338622388 | EPHA2 | c.2244C>A (p.Asn748Lys) c.2082C>A (p.Asn694Lys) | |
1 | g.16132146T>A | CA338622389 | EPHA2 | c.2243A>T (p.Asn748Ile) c.2081A>T (p.Asn694Ile) | |
1 | g.16132146T>C | CA338622390 | EPHA2 | c.2243A>G (p.Asn748Ser) c.2081A>G (p.Asn694Ser) | |
1 | g.16132146T>G | CA338622391 | EPHA2 | c.2243A>C (p.Asn748Thr) c.2081A>C (p.Asn694Thr) | |
1 | g.16132147T>A | CA338622392 | EPHA2 | c.2242A>T (p.Asn748Tyr) c.2080A>T (p.Asn694Tyr) | |
1 | g.16132147T>C | CA338622393 | EPHA2 | c.2242A>G (p.Asn748Asp) c.2080A>G (p.Asn694Asp) | |
1 | g.16132147T>G | CA338622394 | EPHA2 | c.2242A>C (p.Asn748His) c.2080A>C (p.Asn694His) | |
1 | g.16132148G>A | CA624885 | EPHA2 | c.2241C>T (p.Val747=) c.2079C>T (p.Val693=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.16132148G>C | CA416385559 | EPHA2 | c.2241C>G (p.Val747=) c.2079C>G (p.Val693=) | |
1 | g.16132148G= | CA1142346036 | EPHA2 | c.2241C= (p.Val747=) c.2079C= (p.Val693=) | |
1 | g.16132148G>T | CA416385560 | EPHA2 | c.2241C>A (p.Val747=) c.2079C>A (p.Val693=) | |
1 | g.16132149A= | CA1155650068 | EPHA2 | c.2240T= (p.Val747=) c.2078T= (p.Val693=) | |
1 | g.16132149A>C | CA338622396 | EPHA2 | c.2240T>G (p.Val747Gly) c.2078T>G (p.Val693Gly) | |
1 | g.16132149A>G | CA338622397 | EPHA2 | c.2240T>C (p.Val747Ala) c.2078T>C (p.Val693Ala) | dbSNP |
1 | g.16132149A>T | CA338622395 | EPHA2 | c.2240T>A (p.Val747Asp) c.2078T>A (p.Val693Asp) | |
1 | g.16132150C>A | CA338622398 | EPHA2 | c.2239G>T (p.Val747Phe) c.2077G>T (p.Val693Phe) | |
1 | g.16132150C= | CA1142063002 | EPHA2 | c.2239G= (p.Val747=) c.2077G= (p.Val693=) | |
1 | g.16132150C>G | CA338622399 | EPHA2 | c.2239G>C (p.Val747Leu) c.2077G>C (p.Val693Leu) | |
1 | g.16132150C>T | CA624886 | EPHA2 | c.2239G>A (p.Val747Ile) c.2077G>A (p.Val693Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.16132151G>A | CA624887 | EPHA2 | c.2238C>T (p.Leu746=) c.2076C>T (p.Leu692=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.16132151G>C | CA416385562 | EPHA2 | c.2238C>G (p.Leu746=) c.2076C>G (p.Leu692=) | gnomAD v4 |
1 | g.16132151G= | CA1142086851 | EPHA2 | c.2238C= (p.Leu746=) c.2076C= (p.Leu692=) | |
1 | g.16132151G>T | CA416385563 | EPHA2 | c.2238C>A (p.Leu746=) c.2076C>A (p.Leu692=) | gnomAD v4 |
1 | g.16132152A>C | CA338622402 | EPHA2 | c.2237T>G (p.Leu746Arg) c.2075T>G (p.Leu692Arg) | |
1 | g.16132152A>G | CA338622401 | EPHA2 | c.2237T>C (p.Leu746Pro) c.2075T>C (p.Leu692Pro) | |
1 | g.16132152A>T | CA338622400 | EPHA2 | c.2237T>A (p.Leu746His) c.2075T>A (p.Leu692His) | |
1 | g.16132153G>A | CA338622403 | EPHA2 | c.2236C>T (p.Leu746Phe) c.2074C>T (p.Leu692Phe) | |
1 | g.16132153G>C | CA338622404 | EPHA2 | c.2236C>G (p.Leu746Val) c.2074C>G (p.Leu692Val) | |
1 | g.16132153G= | CA1155650080 | EPHA2 | c.2236C= (p.Leu746=) c.2074C= (p.Leu692=) | |
1 | g.16132153G>T | CA624888 | EPHA2 | c.2236C>A (p.Leu746Ile) c.2074C>A (p.Leu692Ile) | dbSNP ExAC gnomAD v2 |
1 | g.16132154G>A | CA416385566 | EPHA2 | c.2235C>T (p.Ile745=) c.2073C>T (p.Ile691=) | ClinVar dbSNP gnomAD v4 |