Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.18599658_18599659delinsTGCA2326433815CRLF1c.303_304delinsCA (p.Ala101=)
c.237_238delinsCA (p.Ala79=)
19g.18599659G>ACA506044614CRLF1c.303C>T (p.Ala101=)
c.237C>T (p.Ala79=)
19g.18599659G>CCA506044615CRLF1c.303C>G (p.Ala101=)
c.237C>G (p.Ala79=)
19g.18599659G>TCA506044616CRLF1c.303C>A (p.Ala101=)
c.237C>A (p.Ala79=)
19g.18599660delCA342061CRLF1c.303del (p.Asn102ThrfsTer?)
c.237del (p.Asn80ThrfsTer?)
dbSNP
19g.18599660G>ACA404851987CRLF1c.302C>T (p.Ala101Val)
c.236C>T (p.Ala79Val)
19g.18599660G>CCA404851988CRLF1c.302C>G (p.Ala101Gly)
c.236C>G (p.Ala79Gly)
19g.18599660G>TCA404851989CRLF1c.302C>A (p.Ala101Asp)
c.236C>A (p.Ala79Asp)
19g.18599661C>ACA404851990CRLF1c.301G>T (p.Ala101Ser)
c.235G>T (p.Ala79Ser)
19g.18599661C=CA2326433816CRLF1c.301G= (p.Ala101=)
c.235G= (p.Ala79=)
19g.18599661C>GCA404851991CRLF1c.301G>C (p.Ala101Pro)
c.235G>C (p.Ala79Pro)
gnomAD v4
19g.18599661C>TCA306262299CRLF1c.301G>A (p.Ala101Thr)
c.235G>A (p.Ala79Thr)
dbSNP gnomAD v3 gnomAD v4
19g.18599662C>ACA506044617CRLF1c.300G>T (p.Leu100=)
c.234G>T (p.Leu78=)
19g.18599662C=CA2326433817CRLF1c.300G= (p.Leu100=)
c.234G= (p.Leu78=)
19g.18599662C>GCA506044618CRLF1c.300G>C (p.Leu100=)
c.234G>C (p.Leu78=)
gnomAD v4
19g.18599662C>TCA9314286CRLF1c.300G>A (p.Leu100=)
c.234G>A (p.Leu78=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.18599663A>CCA404851992CRLF1c.299T>G (p.Leu100Arg)
c.233T>G (p.Leu78Arg)
19g.18599663A>GCA404851993CRLF1c.299T>C (p.Leu100Pro)
c.233T>C (p.Leu78Pro)
COSMIC
19g.18599663A>TCA404851994CRLF1c.299T>A (p.Leu100Gln)
c.233T>A (p.Leu78Gln)
19g.18599664G>ACA506044619CRLF1c.298C>T (p.Leu100=)
c.232C>T (p.Leu78=)
gnomAD v4
19g.18599664G>CCA9314287CRLF1c.298C>G (p.Leu100Val)
c.232C>G (p.Leu78Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.18599664G=CA2326433818CRLF1c.298C= (p.Leu100=)
c.232C= (p.Leu78=)
19g.18599664G>TCA404851995CRLF1c.298C>A (p.Leu100Met)
c.232C>A (p.Leu78Met)
gnomAD v4
19g.18599665G>ACA9314288CRLF1c.297C>T (p.Ala99=)
c.231C>T (p.Ala77=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.18599665G>CCA506044621CRLF1c.297C>G (p.Ala99=)
c.231C>G (p.Ala77=)
19g.18599665G=CA2326433819CRLF1c.297C= (p.Ala99=)
c.231C= (p.Ala77=)
19g.18599665G>TCA506044620CRLF1c.297C>A (p.Ala99=)
c.231C>A (p.Ala77=)
19g.18599666G>ACA404851996CRLF1c.296C>T (p.Ala99Val)
c.230C>T (p.Ala77Val)
19g.18599666G>CCA404851997CRLF1c.296C>G (p.Ala99Gly)
c.230C>G (p.Ala77Gly)
19g.18599666G>TCA404851998CRLF1c.296C>A (p.Ala99Asp)
c.230C>A (p.Ala77Asp)
19g.18599667C>ACA404851999CRLF1c.295G>T (p.Ala99Ser)
c.229G>T (p.Ala77Ser)
19g.18599667C>GCA404852000CRLF1c.295G>C (p.Ala99Pro)
c.229G>C (p.Ala77Pro)
19g.18599667C>TCA404852001CRLF1c.295G>A (p.Ala99Thr)
c.229G>A (p.Ala77Thr)
19g.18599668C>ACA506044623CRLF1c.294G>T (p.Leu98=)
c.228G>T (p.Leu76=)
19g.18599668C>GCA506044625CRLF1c.294G>C (p.Leu98=)
c.228G>C (p.Leu76=)
19g.18599668C>TCA506044624CRLF1c.294G>A (p.Leu98=)
c.228G>A (p.Leu76=)
19g.18599669A>CCA404852004CRLF1c.293T>G (p.Leu98Arg)
c.227T>G (p.Leu76Arg)
19g.18599669A>GCA404852002CRLF1c.293T>C (p.Leu98Pro)
c.227T>C (p.Leu76Pro)
gnomAD v4
19g.18599669A>TCA404852003CRLF1c.293T>A (p.Leu98Gln)
c.227T>A (p.Leu76Gln)
19g.18599670G>ACA9314289CRLF1c.292C>T (p.Leu98=)
c.226C>T (p.Leu76=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.18599670G>CCA404852005CRLF1c.292C>G (p.Leu98Val)
c.226C>G (p.Leu76Val)
19g.18599670G=CA2326433820CRLF1c.292C= (p.Leu98=)
c.226C= (p.Leu76=)
19g.18599670G>TCA404852006CRLF1c.292C>A (p.Leu98Met)
c.226C>A (p.Leu76Met)
19g.18599671A=CA2326433821CRLF1c.291T= (p.Ala97=)
c.225T= (p.Ala75=)
19g.18599671A>CCA506044626CRLF1c.291T>G (p.Ala97=)
c.225T>G (p.Ala75=)
dbSNP gnomAD v2 gnomAD v4
19g.18599671A>GCA506044627CRLF1c.291T>C (p.Ala97=)
c.225T>C (p.Ala75=)
dbSNP
19g.18599671A>TCA506044628CRLF1c.291T>A (p.Ala97=)
c.225T>A (p.Ala75=)
19g.18599672G>ACA404852007CRLF1c.290C>T (p.Ala97Val)
c.224C>T (p.Ala75Val)
gnomAD v4
19g.18599672G>CCA404852008CRLF1c.290C>G (p.Ala97Gly)
c.224C>G (p.Ala75Gly)
19g.18599672G>TCA404852009CRLF1c.290C>A (p.Ala97Asp)
c.224C>A (p.Ala75Asp)

Number of alleles fetched