Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.46894684A>CCA380285463LRP4c.1445T>G (p.Val482Gly)
c.1658T>G (p.Val553Gly)
c.641T>G (p.Val214Gly)
11g.46894684A>GCA380285465LRP4c.1445T>C (p.Val482Ala)
c.1658T>C (p.Val553Ala)
c.641T>C (p.Val214Ala)
11g.46894684A>TCA380285468LRP4c.1445T>A (p.Val482Asp)
c.1658T>A (p.Val553Asp)
c.641T>A (p.Val214Asp)
11g.46894685C>ACA380285471LRP4c.1444G>T (p.Val482Phe)
c.1657G>T (p.Val553Phe)
c.640G>T (p.Val214Phe)
11g.46894685C=CA1969144796LRP4c.1444G= (p.Val482=)
c.1657G= (p.Val553=)
c.640G= (p.Val214=)
11g.46894685C>GCA380285472LRP4c.1444G>C (p.Val482Leu)
c.1657G>C (p.Val553Leu)
c.640G>C (p.Val214Leu)
11g.46894685C>TCA221647359LRP4c.1444G>A (p.Val482Ile)
c.1657G>A (p.Val553Ile)
c.640G>A (p.Val214Ile)
dbSNP gnomAD v4
11g.46894686A>CCA474204967LRP4c.1443T>G (p.Leu481=)
c.1656T>G (p.Leu552=)
c.639T>G (p.Leu213=)
11g.46894686A>GCA474204969LRP4c.1443T>C (p.Leu481=)
c.1656T>C (p.Leu552=)
c.639T>C (p.Leu213=)
dbSNP
11g.46894686A>TCA474204970LRP4c.1443T>A (p.Leu481=)
c.1656T>A (p.Leu552=)
c.639T>A (p.Leu213=)
11g.46894687A>CCA380285484LRP4c.1442T>G (p.Leu481Arg)
c.1655T>G (p.Leu552Arg)
c.638T>G (p.Leu213Arg)
11g.46894687A>GCA380285481LRP4c.1442T>C (p.Leu481Pro)
c.1655T>C (p.Leu552Pro)
c.638T>C (p.Leu213Pro)
11g.46894687A>TCA380285478LRP4c.1442T>A (p.Leu481His)
c.1655T>A (p.Leu552His)
c.638T>A (p.Leu213His)
11g.46894688G>ACA380285487LRP4c.1441C>T (p.Leu481Phe)
c.1654C>T (p.Leu552Phe)
c.637C>T (p.Leu213Phe)
11g.46894688G>CCA380285489LRP4c.1441C>G (p.Leu481Val)
c.1654C>G (p.Leu552Val)
c.637C>G (p.Leu213Val)
11g.46894688G>TCA380285492LRP4c.1441C>A (p.Leu481Ile)
c.1654C>A (p.Leu552Ile)
c.637C>A (p.Leu213Ile)
11g.46894689C>ACA380285496LRP4c.1440G>T (p.Glu480Asp)
c.1653G>T (p.Glu551Asp)
c.636G>T (p.Glu212Asp)
11g.46894689C=CA1969144799LRP4c.1440G= (p.Glu480=)
c.1653G= (p.Glu551=)
c.636G= (p.Glu212=)
11g.46894689C>GCA380285499LRP4c.1440G>C (p.Glu480Asp)
c.1653G>C (p.Glu551Asp)
c.636G>C (p.Glu212Asp)
gnomAD v4
11g.46894689C>TCA474204972LRP4c.1440G>A (p.Glu480=)
c.1653G>A (p.Glu551=)
c.636G>A (p.Glu212=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.46894690T>ACA380285503LRP4c.1439A>T (p.Glu480Val)
c.1652A>T (p.Glu551Val)
c.635A>T (p.Glu212Val)
11g.46894690T>CCA380285506LRP4c.1439A>G (p.Glu480Gly)
c.1652A>G (p.Glu551Gly)
c.635A>G (p.Glu212Gly)
11g.46894690T>GCA380285510LRP4c.1439A>C (p.Glu480Ala)
c.1652A>C (p.Glu551Ala)
c.635A>C (p.Glu212Ala)
11g.46894691C>ACA380285513LRP4c.1438G>T (p.Glu480Ter)
c.1651G>T (p.Glu551Ter)
c.634G>T (p.Glu212Ter)
11g.46894691C=CA1969144805LRP4c.1438G= (p.Glu480=)
c.1651G= (p.Glu551=)
c.634G= (p.Glu212=)
11g.46894691C>GCA5970149LRP4c.1438G>C (p.Glu480Gln)
c.1651G>C (p.Glu551Gln)
c.634G>C (p.Glu212Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894691C>TCA380285516LRP4c.1438G>A (p.Glu480Lys)
c.1651G>A (p.Glu551Lys)
c.634G>A (p.Glu212Lys)
dbSNP gnomAD v4
11g.46894692G>ACA5970150LRP4c.1437C>T (p.Arg479=)
c.1650C>T (p.Arg550=)
c.633C>T (p.Arg211=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894692G>CCA474204973LRP4c.1437C>G (p.Arg479=)
c.1650C>G (p.Arg550=)
c.633C>G (p.Arg211=)
11g.46894692G=CA1969144810LRP4c.1437C= (p.Arg479=)
c.1650C= (p.Arg550=)
c.633C= (p.Arg211=)
11g.46894692G>TCA474204974LRP4c.1437C>A (p.Arg479=)
c.1650C>A (p.Arg550=)
c.633C>A (p.Arg211=)
11g.46894693C>ACA380285523LRP4c.1436G>T (p.Arg479Leu)
c.1649G>T (p.Arg550Leu)
c.632G>T (p.Arg211Leu)
ClinVar dbSNP gnomAD v4
11g.46894693C=CA1969144814LRP4c.1436G= (p.Arg479=)
c.1649G= (p.Arg550=)
c.632G= (p.Arg211=)
11g.46894693C>GCA380285531LRP4c.1436G>C (p.Arg479Pro)
c.1649G>C (p.Arg550Pro)
c.632G>C (p.Arg211Pro)
11g.46894693C>TCA5970151LRP4c.1436G>A (p.Arg479His)
c.1649G>A (p.Arg550His)
c.632G>A (p.Arg211His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.46894694G>ACA5970152LRP4c.1435C>T (p.Arg479Cys)
c.1648C>T (p.Arg550Cys)
c.631C>T (p.Arg211Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894694G>CCA380285537LRP4c.1435C>G (p.Arg479Gly)
c.1648C>G (p.Arg550Gly)
c.631C>G (p.Arg211Gly)
11g.46894694G=CA1969144823LRP4c.1435C= (p.Arg479=)
c.1648C= (p.Arg550=)
c.631C= (p.Arg211=)
11g.46894694G>TCA380285540LRP4c.1435C>A (p.Arg479Ser)
c.1648C>A (p.Arg550Ser)
c.631C>A (p.Arg211Ser)
11g.46894695G>ACA221647401LRP4c.1434C>T (p.Arg478=)
c.1647C>T (p.Arg549=)
c.630C>T (p.Arg210=)
dbSNP gnomAD v3 gnomAD v4
11g.46894695G>CCA474204975LRP4c.1434C>G (p.Arg478=)
c.1647C>G (p.Arg549=)
c.630C>G (p.Arg210=)
11g.46894695G=CA1969144833LRP4c.1434C= (p.Arg478=)
c.1647C= (p.Arg549=)
c.630C= (p.Arg210=)
11g.46894695G>TCA474204976LRP4c.1434C>A (p.Arg478=)
c.1647C>A (p.Arg549=)
c.630C>A (p.Arg210=)
11g.46894696C>ACA380285543LRP4c.1433G>T (p.Arg478Leu)
c.1646G>T (p.Arg549Leu)
c.629G>T (p.Arg210Leu)
11g.46894696C=CA1969144836LRP4c.1433G= (p.Arg478=)
c.1646G= (p.Arg549=)
c.629G= (p.Arg210=)
11g.46894696C>GCA380285545LRP4c.1433G>C (p.Arg478Pro)
c.1646G>C (p.Arg549Pro)
c.629G>C (p.Arg210Pro)
11g.46894696C>TCA380285548LRP4c.1433G>A (p.Arg478His)
c.1646G>A (p.Arg549His)
c.629G>A (p.Arg210His)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.46894697G>ACA5970153LRP4c.1432C>T (p.Arg478Cys)
c.1645C>T (p.Arg549Cys)
c.628C>T (p.Arg210Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894697G>CCA380285550LRP4c.1432C>G (p.Arg478Gly)
c.1645C>G (p.Arg549Gly)
c.628C>G (p.Arg210Gly)
11g.46894697G=CA1969144840LRP4c.1432C= (p.Arg478=)
c.1645C= (p.Arg549=)
c.628C= (p.Arg210=)

Number of alleles fetched