Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.68347958_68347968delinsTGGACTTCCAGCA1980629765LRP5c.203_213delinsTGGACTTCCAG (p.Val68=)
c.-1563_-1553delinsTGGACTTCCAG (n.-1563_-1553delinsTGGACTTCCAG)
c.230_240delinsTGGACTTCCAG (p.Val77=)
n.245_255delinsTGGACTTCCAG
11g.68347959_68347968delCA600238881LRP5c.204_213del (p.Asp69PhefsTer11)
c.-1562_-1553del (n.-1562_-1553del)
c.231_240del (p.Asp78PhefsTer11)
n.246_255del
ClinVar dbSNP gnomAD v2
11g.68347960G>ACA381610277LRP5c.205G>A (p.Asp69Asn)
c.-1561G>A (n.-1561G>A)
c.232G>A (p.Asp78Asn)
n.247G>A
11g.68347960G>CCA381610278LRP5c.205G>C (p.Asp69His)
c.-1561G>C (n.-1561G>C)
c.232G>C (p.Asp78His)
n.247G>C
11g.68347960G=CA1980629776LRP5c.205G= (p.Asp69=)
c.-1561G= (n.-1561G=)
c.232G= (p.Asp78=)
n.247G=
11g.68347960G>TCA16044353LRP5c.205G>T (p.Asp69Tyr)
c.-1561G>T (n.-1561G>T)
c.232G>T (p.Asp78Tyr)
n.247G>T
ClinVar dbSNP
11g.68347961A>CCA381610279LRP5c.206A>C (p.Asp69Ala)
c.-1560A>C (n.-1560A>C)
c.233A>C (p.Asp78Ala)
n.248A>C
11g.68347961A>GCA381610280LRP5c.206A>G (p.Asp69Gly)
c.-1560A>G (n.-1560A>G)
c.233A>G (p.Asp78Gly)
n.248A>G
11g.68347961A>TCA381610281LRP5c.206A>T (p.Asp69Val)
c.-1560A>T (n.-1560A>T)
c.233A>T (p.Asp78Val)
n.248A>T
11g.68347962C>ACA381610282LRP5c.207C>A (p.Asp69Glu)
c.-1559C>A (n.-1559C>A)
c.234C>A (p.Asp78Glu)
n.249C>A
dbSNP
11g.68347962C>GCA381610283LRP5c.207C>G (p.Asp69Glu)
c.-1559C>G (n.-1559C>G)
c.234C>G (p.Asp78Glu)
n.249C>G
11g.68347962C>TCA475516765LRP5c.207C>T (p.Asp69=)
c.-1559C>T (n.-1559C>T)
c.234C>T (p.Asp78=)
n.249C>T
gnomAD v4
11g.68347963T>ACA381610284LRP5c.208T>A (p.Phe70Ile)
c.-1558T>A (n.-1558T>A)
c.235T>A (p.Phe79Ile)
n.250T>A
11g.68347963T>CCA381610285LRP5c.208T>C (p.Phe70Leu)
c.-1558T>C (n.-1558T>C)
c.235T>C (p.Phe79Leu)
n.250T>C
11g.68347963T>GCA381610286LRP5c.208T>G (p.Phe70Val)
c.-1558T>G (n.-1558T>G)
c.235T>G (p.Phe79Val)
n.250T>G
11g.68347964T>ACA381610287LRP5c.209T>A (p.Phe70Tyr)
c.-1557T>A (n.-1557T>A)
c.236T>A (p.Phe79Tyr)
n.251T>A
ClinVar dbSNP gnomAD v4
11g.68347964T>CCA381610288LRP5c.209T>C (p.Phe70Ser)
c.-1557T>C (n.-1557T>C)
c.236T>C (p.Phe79Ser)
n.251T>C
11g.68347964T>GCA381610289LRP5c.209T>G (p.Phe70Cys)
c.-1557T>G (n.-1557T>G)
c.236T>G (p.Phe79Cys)
n.251T>G
11g.68347964_68347965delinsAACA916083252LRP5c.209_210delinsAA (p.Phe70Ter)
c.-1557_-1556delinsAA (n.-1557_-1556delinsAA)
c.236_237delinsAA (p.Phe79Ter)
n.251_252delinsAA
ClinVar dbSNP
11g.68347964_68347965delinsTCCA1980629784LRP5c.209_210delinsTC (p.Phe70=)
c.-1557_-1556delinsTC (n.-1557_-1556delinsTC)
c.236_237delinsTC (p.Phe79=)
n.251_252delinsTC
11g.68347965C>ACA381610290LRP5c.210C>A (p.Phe70Leu)
c.-1556C>A (n.-1556C>A)
c.237C>A (p.Phe79Leu)
n.252C>A
ClinVar dbSNP gnomAD v4
11g.68347965C=CA1980629790LRP5c.210C= (p.Phe70=)
c.-1556C= (n.-1556C=)
c.237C= (p.Phe79=)
n.252C=
11g.68347965C>GCA381610291LRP5c.210C>G (p.Phe70Leu)
c.-1556C>G (n.-1556C>G)
c.237C>G (p.Phe79Leu)
n.252C>G
11g.68347965C>TCA6148935LRP5c.210C>T (p.Phe70=)
c.-1556C>T (n.-1556C>T)
c.237C>T (p.Phe79=)
n.252C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68347966C>ACA381610292LRP5c.211C>A (p.Gln71Lys)
c.-1555C>A (n.-1555C>A)
c.238C>A (p.Gln80Lys)
n.253C>A
11g.68347966C>GCA381610294LRP5c.211C>G (p.Gln71Glu)
c.-1555C>G (n.-1555C>G)
c.238C>G (p.Gln80Glu)
n.253C>G
11g.68347966C>TCA381610293LRP5c.211C>T (p.Gln71Ter)
c.-1555C>T (n.-1555C>T)
c.238C>T (p.Gln80Ter)
n.253C>T
gnomAD v4
11g.68347967A=CA1980629795LRP5c.212A= (p.Gln71=)
c.-1554A= (n.-1554A=)
c.239A= (p.Gln80=)
n.254A=
11g.68347967A>CCA381610295LRP5c.212A>C (p.Gln71Pro)
c.-1554A>C (n.-1554A>C)
c.239A>C (p.Gln80Pro)
n.254A>C
gnomAD v4
11g.68347967A>GCA6148936LRP5c.212A>G (p.Gln71Arg)
c.-1554A>G (n.-1554A>G)
c.239A>G (p.Gln80Arg)
n.254A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.68347967A>TCA381610296LRP5c.212A>T (p.Gln71Leu)
c.-1554A>T (n.-1554A>T)
c.239A>T (p.Gln80Leu)
n.254A>T
11g.68347968G>ACA475516770LRP5c.213G>A (p.Gln71=)
c.-1553G>A (n.-1553G>A)
c.240G>A (p.Gln80=)
n.255G>A
11g.68347968G>CCA381610297LRP5c.213G>C (p.Gln71His)
c.-1553G>C (n.-1553G>C)
c.240G>C (p.Gln80His)
n.255G>C
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.68347968G=CA1980629800LRP5c.213G= (p.Gln71=)
c.-1553G= (n.-1553G=)
c.240G= (p.Gln80=)
n.255G=
11g.68347968G>TCA381610298LRP5c.213G>T (p.Gln71His)
c.-1553G>T (n.-1553G>T)
c.240G>T (p.Gln80His)
n.255G>T
11g.68347969T>ACA381610299LRP5c.214T>A (p.Phe72Ile)
c.-1552T>A (n.-1552T>A)
c.241T>A (p.Phe81Ile)
n.256T>A
11g.68347969T>CCA381610300LRP5c.214T>C (p.Phe72Leu)
c.-1552T>C (n.-1552T>C)
c.241T>C (p.Phe81Leu)
n.256T>C
gnomAD v4
11g.68347969T>GCA381610301LRP5c.214T>G (p.Phe72Val)
c.-1552T>G (n.-1552T>G)
c.241T>G (p.Phe81Val)
n.256T>G
11g.68347970T>ACA381610302LRP5c.215T>A (p.Phe72Tyr)
c.-1551T>A (n.-1551T>A)
c.242T>A (p.Phe81Tyr)
n.257T>A
11g.68347970T>CCA381610303LRP5c.215T>C (p.Phe72Ser)
c.-1551T>C (n.-1551T>C)
c.242T>C (p.Phe81Ser)
n.257T>C
gnomAD v4
11g.68347970T>GCA381610304LRP5c.215T>G (p.Phe72Cys)
c.-1551T>G (n.-1551T>G)
c.242T>G (p.Phe81Cys)
n.257T>G
11g.68347971T>ACA381610305LRP5c.216T>A (p.Phe72Leu)
c.-1550T>A (n.-1550T>A)
c.243T>A (p.Phe81Leu)
n.258T>A
11g.68347971T>CCA475516772LRP5c.216T>C (p.Phe72=)
c.-1550T>C (n.-1550T>C)
c.243T>C (p.Phe81=)
n.258T>C
11g.68347971T>GCA381610306LRP5c.216T>G (p.Phe72Leu)
c.-1550T>G (n.-1550T>G)
c.243T>G (p.Phe81Leu)
n.258T>G
11g.68347972T>ACA381610307LRP5c.217T>A (p.Ser73Thr)
c.-1549T>A (n.-1549T>A)
c.244T>A (p.Ser82Thr)
n.259T>A
11g.68347972T>CCA381610308LRP5c.217T>C (p.Ser73Pro)
c.-1549T>C (n.-1549T>C)
c.244T>C (p.Ser82Pro)
n.259T>C
11g.68347972T>GCA381610309LRP5c.217T>G (p.Ser73Ala)
c.-1549T>G (n.-1549T>G)
c.244T>G (p.Ser82Ala)
n.259T>G
gnomAD v4
11g.68347973C>ACA381610310LRP5c.218C>A (p.Ser73Tyr)
c.-1548C>A (n.-1548C>A)
c.245C>A (p.Ser82Tyr)
n.260C>A
11g.68347973C=CA1980629810LRP5c.218C= (p.Ser73=)
c.-1548C= (n.-1548C=)
c.245C= (p.Ser82=)
n.260C=
11g.68347973C>GCA381610312LRP5c.218C>G (p.Ser73Cys)
c.-1548C>G (n.-1548C>G)
c.245C>G (p.Ser82Cys)
n.260C>G

Number of alleles fetched