Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.86890052_86890075delCA2695212250BMPR1Ac.68-10_81del
10g.86890065A=CA1925720264BMPR1Ac.71A= (p.Gln24=)
10g.86890065A>CCA377446216BMPR1Ac.71A>C (p.Gln24Pro)
10g.86890065A>GCA377446217BMPR1Ac.71A>G (p.Gln24Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
10g.86890065A>TCA377446219BMPR1Ac.71A>T (p.Gln24Leu)
ClinVar dbSNP
10g.86890066_86890067delCA2695212251BMPR1Ac.72_73del (p.Asn25SerfsTer3)
10g.86890066G>ACA5585429BMPR1Ac.72G>A (p.Gln24=)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.86890066G>CCA377446222BMPR1Ac.72G>C (p.Gln24His)
10g.86890066G=CA1925720276BMPR1Ac.72G= (p.Gln24=)
10g.86890066G>TCA377446223BMPR1Ac.72G>T (p.Gln24His)
10g.86890067A>CCA377446229BMPR1Ac.73A>C (p.Asn25His)
10g.86890067A>GCA377446227BMPR1Ac.73A>G (p.Asn25Asp)
10g.86890067A>TCA377446225BMPR1Ac.73A>T (p.Asn25Tyr)
10g.86890068A=CA1925720281BMPR1Ac.74A= (p.Asn25=)
10g.86890068A>CCA377446231BMPR1Ac.74A>C (p.Asn25Thr)
ClinVar dbSNP
10g.86890068A>GCA16613192BMPR1Ac.74A>G (p.Asn25Ser)
ClinVar dbSNP gnomAD v3 gnomAD v4
10g.86890068A>TCA377446234BMPR1Ac.74A>T (p.Asn25Ile)
10g.86890069T>ACA377446236BMPR1Ac.75T>A (p.Asn25Lys)
10g.86890069T>CCA470304474BMPR1Ac.75T>C (p.Asn25=)
10g.86890069T>GCA377446237BMPR1Ac.75T>G (p.Asn25Lys)
gnomAD v4
10g.86890070C>ACA377446238BMPR1Ac.76C>A (p.Leu26Met)
10g.86890070C>GCA377446240BMPR1Ac.76C>G (p.Leu26Val)
gnomAD v4
10g.86890070C>TCA470304475BMPR1Ac.76C>T (p.Leu26=)
10g.86890071T>ACA377446243BMPR1Ac.77T>A (p.Leu26Gln)
10g.86890071T>CCA211182656BMPR1Ac.77T>C (p.Leu26Pro)
dbSNP
10g.86890071T>GCA377446244BMPR1Ac.77T>G (p.Leu26Arg)
10g.86890071T=CA1925720286BMPR1Ac.77T= (p.Leu26=)
10g.86890072G>ACA470304477BMPR1Ac.78G>A (p.Leu26=)
10g.86890072G>CCA470304478BMPR1Ac.78G>C (p.Leu26=)
10g.86890072G>TCA470304479BMPR1Ac.78G>T (p.Leu26=)
10g.86890073_86890077delCA2695200862BMPR1Ac.79_83del (p.Asp27TyrfsTer?)
10g.86890073G>ACA377446246BMPR1Ac.79G>A (p.Asp27Asn)
gnomAD v4
10g.86890073G>CCA377446248BMPR1Ac.79G>C (p.Asp27His)
10g.86890073G=CA1925720291BMPR1Ac.79G= (p.Asp27=)
10g.86890073G>TCA377446249BMPR1Ac.79G>T (p.Asp27Tyr)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.86890074A=CA1925720298BMPR1Ac.80A= (p.Asp27=)
10g.86890074A>CCA377446257BMPR1Ac.80A>C (p.Asp27Ala)
10g.86890074A>GCA377446254BMPR1Ac.80A>G (p.Asp27Gly)
ClinVar dbSNP
10g.86890074A>TCA377446251BMPR1Ac.80A>T (p.Asp27Val)
10g.86890075T>ACA377446259BMPR1Ac.81T>A (p.Asp27Glu)
10g.86890075T>CCA470304480BMPR1Ac.81T>C (p.Asp27=)
ClinVar dbSNP
10g.86890075T>GCA377446261BMPR1Ac.81T>G (p.Asp27Glu)
10g.86890075T=CA1925720301BMPR1Ac.81T= (p.Asp27=)
10g.86890076A=CA1925720306BMPR1Ac.82A= (p.Ser28=)
10g.86890076A>CCA377446263BMPR1Ac.82A>C (p.Ser28Arg)
10g.86890076A>GCA377446265BMPR1Ac.82A>G (p.Ser28Gly)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.86890076A>TCA377446268BMPR1Ac.82A>T (p.Ser28Cys)
10g.86890077G>ACA336464BMPR1Ac.83G>A (p.Ser28Asn)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.86890077G>CCA377446271BMPR1Ac.83G>C (p.Ser28Thr)
10g.86890077G=CA1925720310BMPR1Ac.83G= (p.Ser28=)

Number of alleles fetched