Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.28900749A>CCA395411255ATP2A1c.1933A>C (p.Asn645His)
c.1558A>C (p.Asn520His)
16g.28900749A>GCA395411254ATP2A1c.1933A>G (p.Asn645Asp)
c.1558A>G (p.Asn520Asp)
16g.28900749A>TCA395411253ATP2A1c.1933A>T (p.Asn645Tyr)
c.1558A>T (p.Asn520Tyr)
16g.28900750A>CCA395411256ATP2A1c.1934A>C (p.Asn645Thr)
c.1559A>C (p.Asn520Thr)
16g.28900750A>GCA395411257ATP2A1c.1934A>G (p.Asn645Ser)
c.1559A>G (p.Asn520Ser)
16g.28900750A>TCA395411258ATP2A1c.1934A>T (p.Asn645Ile)
c.1559A>T (p.Asn520Ile)
16g.28900751C>ACA395411259ATP2A1c.1935C>A (p.Asn645Lys)
c.1560C>A (p.Asn520Lys)
16g.28900751C=CA2215884885ATP2A1c.1935C= (p.Asn645=)
c.1560C= (p.Asn520=)
16g.28900751C>GCA395411260ATP2A1c.1935C>G (p.Asn645Lys)
c.1560C>G (p.Asn520Lys)
16g.28900751C>TCA7987120ATP2A1c.1935C>T (p.Asn645=)
c.1560C>T (p.Asn520=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.28900752G>ACA7987121ATP2A1c.1936G>A (p.Glu646Lys)
c.1561G>A (p.Glu521Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900752G>CCA7987122ATP2A1c.1936G>C (p.Glu646Gln)
c.1561G>C (p.Glu521Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.28900752G=CA2215884907ATP2A1c.1936G= (p.Glu646=)
c.1561G= (p.Glu521=)
16g.28900752G>TCA395411261ATP2A1c.1936G>T (p.Glu646Ter)
c.1561G>T (p.Glu521Ter)
16g.28900756_28900758delCA645573195ATP2A1c.1940_1942del (p.Glu647del)
c.1565_1567del (p.Glu522del)
COSMIC COSMIC
16g.28900753A>CCA395411262ATP2A1c.1937A>C (p.Glu646Ala)
c.1562A>C (p.Glu521Ala)
16g.28900753A>GCA395411263ATP2A1c.1937A>G (p.Glu646Gly)
c.1562A>G (p.Glu521Gly)
16g.28900753A>TCA395411264ATP2A1c.1937A>T (p.Glu646Val)
c.1562A>T (p.Glu521Val)
16g.28900754G>ACA494874387ATP2A1c.1938G>A (p.Glu646=)
c.1563G>A (p.Glu521=)
dbSNP
16g.28900754G>CCA395411265ATP2A1c.1938G>C (p.Glu646Asp)
c.1563G>C (p.Glu521Asp)
ClinVar
16g.28900754G=CA2215884917ATP2A1c.1938G= (p.Glu646=)
c.1563G= (p.Glu521=)
16g.28900754G>TCA395411266ATP2A1c.1938G>T (p.Glu646Asp)
c.1563G>T (p.Glu521Asp)
16g.28900755G>ACA395411267ATP2A1c.1939G>A (p.Glu647Lys)
c.1564G>A (p.Glu522Lys)
gnomAD v4
16g.28900755G>CCA395411268ATP2A1c.1939G>C (p.Glu647Gln)
c.1564G>C (p.Glu522Gln)
16g.28900755G>TCA395411269ATP2A1c.1939G>T (p.Glu647Ter)
c.1564G>T (p.Glu522Ter)
16g.28900756A>CCA395411270ATP2A1c.1940A>C (p.Glu647Ala)
c.1565A>C (p.Glu522Ala)
16g.28900756A>GCA395411271ATP2A1c.1940A>G (p.Glu647Gly)
c.1565A>G (p.Glu522Gly)
16g.28900756A>TCA395411272ATP2A1c.1940A>T (p.Glu647Val)
c.1565A>T (p.Glu522Val)
gnomAD v4
16g.28900757G>ACA10643415ATP2A1c.1941G>A (p.Glu647=)
c.1566G>A (p.Glu522=)
ClinVar dbSNP gnomAD v4
16g.28900757G>CCA395411274ATP2A1c.1941G>C (p.Glu647Asp)
c.1566G>C (p.Glu522Asp)
16g.28900757G=CA2215884921ATP2A1c.1941G= (p.Glu647=)
c.1566G= (p.Glu522=)
16g.28900757G>TCA395411273ATP2A1c.1941G>T (p.Glu647Asp)
c.1566G>T (p.Glu522Asp)
16g.28900758G>ACA395411275ATP2A1c.1942G>A (p.Val648Met)
c.1567G>A (p.Val523Met)
dbSNP gnomAD v3 gnomAD v4
16g.28900758G>CCA395411277ATP2A1c.1942G>C (p.Val648Leu)
c.1567G>C (p.Val523Leu)
16g.28900758G=CA2215884925ATP2A1c.1942G= (p.Val648=)
c.1567G= (p.Val523=)
16g.28900758G>TCA395411276ATP2A1c.1942G>T (p.Val648Leu)
c.1567G>T (p.Val523Leu)
16g.28900759T>ACA395411278ATP2A1c.1943T>A (p.Val648Glu)
c.1568T>A (p.Val523Glu)
16g.28900759T>CCA395411280ATP2A1c.1943T>C (p.Val648Ala)
c.1568T>C (p.Val523Ala)
16g.28900759T>GCA395411279ATP2A1c.1943T>G (p.Val648Gly)
c.1568T>G (p.Val523Gly)
16g.28900760G>ACA494874388ATP2A1c.1944G>A (p.Val648=)
c.1569G>A (p.Val523=)
16g.28900760G>CCA494874389ATP2A1c.1944G>C (p.Val648=)
c.1569G>C (p.Val523=)
16g.28900760G>TCA494874390ATP2A1c.1944G>T (p.Val648=)
c.1569G>T (p.Val523=)
16g.28900761G>ACA395411281ATP2A1c.1945G>A (p.Ala649Thr)
c.1570G>A (p.Ala524Thr)
dbSNP
16g.28900761G>CCA395411282ATP2A1c.1945G>C (p.Ala649Pro)
c.1570G>C (p.Ala524Pro)
16g.28900761G=CA2215884932ATP2A1c.1945G= (p.Ala649=)
c.1570G= (p.Ala524=)
16g.28900761G>TCA395411283ATP2A1c.1945G>T (p.Ala649Ser)
c.1570G>T (p.Ala524Ser)
16g.28900762C>ACA395411284ATP2A1c.1946C>A (p.Ala649Asp)
c.1571C>A (p.Ala524Asp)
16g.28900762C=CA2215884936ATP2A1c.1946C= (p.Ala649=)
c.1571C= (p.Ala524=)
16g.28900762C>GCA395411285ATP2A1c.1946C>G (p.Ala649Gly)
c.1571C>G (p.Ala524Gly)
16g.28900762C>TCA395411286ATP2A1c.1946C>T (p.Ala649Val)
c.1571C>T (p.Ala524Val)
dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched