Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.88732415T>ACA397109799HSALR1,PIEZO1c.2911A>T (p.Thr971Ser)
n.269+967T>A
16g.88732415T>CCA286420401HSALR1,PIEZO1c.2911A>G (p.Thr971Ala)
n.269+967T>C
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88732415T>GCA8232674HSALR1,PIEZO1c.2911A>C (p.Thr971Pro)
n.269+967T>G
dbSNP ExAC gnomAD v2 gnomAD v4
16g.88732415T=CA2241261074HSALR1,PIEZO1c.2911A= (p.Thr971=)
n.269+967T=
16g.88732416G>ACA497366361HSALR1,PIEZO1c.2910C>T (p.Gly970=)
n.269+968G>A
dbSNP gnomAD v2 gnomAD v4
16g.88732416G>CCA497366362HSALR1,PIEZO1c.2910C>G (p.Gly970=)
n.269+968G>C
gnomAD v4
16g.88732416G=CA2241261075HSALR1,PIEZO1c.2910C= (p.Gly970=)
n.269+968G=
16g.88732416G>TCA497366363HSALR1,PIEZO1c.2910C>A (p.Gly970=)
n.269+968G>T
dbSNP gnomAD v2 gnomAD v4
16g.88732417C>ACA397109805HSALR1,PIEZO1c.2909G>T (p.Gly970Val)
n.269+969C>A
16g.88732417C=CA2241261076HSALR1,PIEZO1c.2909G= (p.Gly970=)
n.269+969C=
16g.88732417C>GCA397109808HSALR1,PIEZO1c.2909G>C (p.Gly970Ala)
n.269+969C>G
16g.88732417C>TCA8232675HSALR1,PIEZO1c.2909G>A (p.Gly970Asp)
n.269+969C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88732418C>ACA397109813HSALR1,PIEZO1c.2908G>T (p.Gly970Cys)
n.269+970C>A
gnomAD v4
16g.88732418C=CA2241261077HSALR1,PIEZO1c.2908G= (p.Gly970=)
n.269+970C=
16g.88732418C>GCA397109811HSALR1,PIEZO1c.2908G>C (p.Gly970Arg)
n.269+970C>G
ClinVar dbSNP gnomAD v4
16g.88732418C>TCA286420407HSALR1,PIEZO1c.2908G>A (p.Gly970Ser)
n.269+970C>T
dbSNP gnomAD v2 gnomAD v4 COSMIC
16g.88732419G>ACA8232676HSALR1,PIEZO1c.2907C>T (p.Ser969=)
n.269+971G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.88732419G>CCA397109817HSALR1,PIEZO1c.2907C>G (p.Ser969Arg)
n.269+971G>C
dbSNP gnomAD v2 gnomAD v4
16g.88732419G=CA2241261078HSALR1,PIEZO1c.2907C= (p.Ser969=)
n.269+971G=
16g.88732419G>TCA286420410HSALR1,PIEZO1c.2907C>A (p.Ser969Arg)
n.269+971G>T
dbSNP gnomAD v2 gnomAD v4
16g.88732420C>ACA397109821HSALR1,PIEZO1c.2906G>T (p.Ser969Ile)
n.269+972C>A
16g.88732420C=CA2241261079HSALR1,PIEZO1c.2906G= (p.Ser969=)
n.269+972C=
16g.88732420C>GCA397109822HSALR1,PIEZO1c.2906G>C (p.Ser969Thr)
n.269+972C>G
gnomAD v4
16g.88732420C>TCA397109824HSALR1,PIEZO1c.2906G>A (p.Ser969Asn)
n.269+972C>T
dbSNP gnomAD v2 gnomAD v4
16g.88732421T>ACA397109826HSALR1,PIEZO1c.2905A>T (p.Ser969Cys)
n.269+973T>A
gnomAD v4
16g.88732421T>CCA397109827HSALR1,PIEZO1c.2905A>G (p.Ser969Gly)
n.269+973T>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.88732421T>GCA397109828HSALR1,PIEZO1c.2905A>C (p.Ser969Arg)
n.269+973T>G
16g.88732421T=CA2241261081HSALR1,PIEZO1c.2905A= (p.Ser969=)
n.269+973T=
16g.88732421_88732422delinsTGCA2241261080HSALR1,PIEZO1c.2904_2905delinsCA (p.Ala968=)
n.269+973_269+974delinsTG
16g.88732422G>ACA497366375HSALR1,PIEZO1c.2904C>T (p.Ala968=)
n.269+974G>A
dbSNP gnomAD v2 gnomAD v4
16g.88732422G>CCA497366380HSALR1,PIEZO1c.2904C>G (p.Ala968=)
n.269+974G>C
16g.88732422G=CA2241261082HSALR1,PIEZO1c.2904C= (p.Ala968=)
n.269+974G=
16g.88732422G>TCA497366378HSALR1,PIEZO1c.2904C>A (p.Ala968=)
n.269+974G>T
dbSNP
16g.88732423delCA624449431HSALR1,PIEZO1c.2904del (p.Ser969AlafsTer?)
n.269+975del
dbSNP gnomAD v2 gnomAD v4
16g.88732423G>ACA397109829HSALR1,PIEZO1c.2903C>T (p.Ala968Val)
n.269+975G>A
dbSNP gnomAD v2 gnomAD v4
16g.88732423G>CCA397109831HSALR1,PIEZO1c.2903C>G (p.Ala968Gly)
n.269+975G>C
16g.88732423G=CA2241261083HSALR1,PIEZO1c.2903C= (p.Ala968=)
n.269+975G=
16g.88732423G>TCA397109832HSALR1,PIEZO1c.2903C>A (p.Ala968Asp)
n.269+975G>T
16g.88732424C>ACA397109843HSALR1,PIEZO1c.2902G>T (p.Ala968Ser)
n.269+976C>A
16g.88732424C=CA2241261084HSALR1,PIEZO1c.2902G= (p.Ala968=)
n.269+976C=
16g.88732424C>GCA286420414HSALR1,PIEZO1c.2902G>C (p.Ala968Pro)
n.269+976C>G
dbSNP gnomAD v4
16g.88732424C>TCA397109840HSALR1,PIEZO1c.2902G>A (p.Ala968Thr)
n.269+976C>T
gnomAD v4
16g.88732425A=CA2241261085HSALR1,PIEZO1c.2901T= (p.Phe967=)
n.269+977A=
16g.88732425A>CCA397109847HSALR1,PIEZO1c.2901T>G (p.Phe967Leu)
n.269+977A>C
dbSNP gnomAD v2 gnomAD v4
16g.88732425A>GCA497366389HSALR1,PIEZO1c.2901T>C (p.Phe967=)
n.269+977A>G
16g.88732425A>TCA286420431HSALR1,PIEZO1c.2901T>A (p.Phe967Leu)
n.269+977A>T
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88732426A>CCA397109849HSALR1,PIEZO1c.2900T>G (p.Phe967Cys)
n.269+978A>C
16g.88732426A>GCA397109851HSALR1,PIEZO1c.2900T>C (p.Phe967Ser)
n.269+978A>G
16g.88732426A>TCA397109852HSALR1,PIEZO1c.2900T>A (p.Phe967Tyr)
n.269+978A>T
16g.88732427A=CA2241261086HSALR1,PIEZO1c.2899T= (p.Phe967=)
n.269+979A=

Number of alleles fetched