Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.16828826_16828848delCA2574500155CUBNc.10721_10743del (p.Gly3574ValfsTer28)
c.6707_6729del (p.Gly2236ValfsTer28)
c.6683_6705del (p.Gly2228ValfsTer28)
c.6563_6585del (p.Gly2188ValfsTer28)
10g.16828828A>CCA376119804CUBNc.10741T>G (p.Ser3581Ala)
c.6727T>G (p.Ser2243Ala)
c.6703T>G (p.Ser2235Ala)
c.6583T>G (p.Ser2195Ala)
10g.16828828A>GCA376119806CUBNc.10741T>C (p.Ser3581Pro)
c.6727T>C (p.Ser2243Pro)
c.6703T>C (p.Ser2235Pro)
c.6583T>C (p.Ser2195Pro)
10g.16828828A>TCA376119808CUBNc.10741T>A (p.Ser3581Thr)
c.6727T>A (p.Ser2243Thr)
c.6703T>A (p.Ser2235Thr)
c.6583T>A (p.Ser2195Thr)
10g.16828829T>ACA468407456CUBNc.10740A>T (p.Pro3580=)
c.6726A>T (p.Pro2242=)
c.6702A>T (p.Pro2234=)
c.6582A>T (p.Pro2194=)
10g.16828829T>CCA468407457CUBNc.10740A>G (p.Pro3580=)
c.6726A>G (p.Pro2242=)
c.6702A>G (p.Pro2234=)
c.6582A>G (p.Pro2194=)
10g.16828829T>GCA468407458CUBNc.10740A>C (p.Pro3580=)
c.6726A>C (p.Pro2242=)
c.6702A>C (p.Pro2234=)
c.6582A>C (p.Pro2194=)
10g.16828830G>ACA376119810CUBNc.10739C>T (p.Pro3580Leu)
c.6725C>T (p.Pro2242Leu)
c.6701C>T (p.Pro2234Leu)
c.6581C>T (p.Pro2194Leu)
gnomAD v4
10g.16828830G>CCA376119812CUBNc.10739C>G (p.Pro3580Arg)
c.6725C>G (p.Pro2242Arg)
c.6701C>G (p.Pro2234Arg)
c.6581C>G (p.Pro2194Arg)
10g.16828830G>TCA376119809CUBNc.10739C>A (p.Pro3580Gln)
c.6725C>A (p.Pro2242Gln)
c.6701C>A (p.Pro2234Gln)
c.6581C>A (p.Pro2194Gln)
10g.16828831G>ACA376119814CUBNc.10738C>T (p.Pro3580Ser)
c.6724C>T (p.Pro2242Ser)
c.6700C>T (p.Pro2234Ser)
c.6580C>T (p.Pro2194Ser)
10g.16828831G>CCA203533545CUBNc.10738C>G (p.Pro3580Ala)
c.6724C>G (p.Pro2242Ala)
c.6700C>G (p.Pro2234Ala)
c.6580C>G (p.Pro2194Ala)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.16828831G=CA1893313745CUBNc.10738C= (p.Pro3580=)
c.6724C= (p.Pro2242=)
c.6700C= (p.Pro2234=)
c.6580C= (p.Pro2194=)
10g.16828831G>TCA376119816CUBNc.10738C>A (p.Pro3580Thr)
c.6724C>A (p.Pro2242Thr)
c.6700C>A (p.Pro2234Thr)
c.6580C>A (p.Pro2194Thr)
10g.16828832A=CA1893313748CUBNc.10737T= (p.Ser3579=)
c.6723T= (p.Ser2241=)
c.6699T= (p.Ser2233=)
c.6579T= (p.Ser2193=)
10g.16828832A>CCA468407464CUBNc.10737T>G (p.Ser3579=)
c.6723T>G (p.Ser2241=)
c.6699T>G (p.Ser2233=)
c.6579T>G (p.Ser2193=)
10g.16828832A>GCA468407465CUBNc.10737T>C (p.Ser3579=)
c.6723T>C (p.Ser2241=)
c.6699T>C (p.Ser2233=)
c.6579T>C (p.Ser2193=)
10g.16828832A>TCA203533546CUBNc.10737T>A (p.Ser3579=)
c.6723T>A (p.Ser2241=)
c.6699T>A (p.Ser2233=)
c.6579T>A (p.Ser2193=)
dbSNP
10g.16828833G>ACA5422309CUBNc.10736C>T (p.Ser3579Phe)
c.6722C>T (p.Ser2241Phe)
c.6698C>T (p.Ser2233Phe)
c.6578C>T (p.Ser2193Phe)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.16828833G>CCA376119819CUBNc.10736C>G (p.Ser3579Cys)
c.6722C>G (p.Ser2241Cys)
c.6698C>G (p.Ser2233Cys)
c.6578C>G (p.Ser2193Cys)
dbSNP gnomAD v3 gnomAD v4
10g.16828833G=CA1893313753CUBNc.10736C= (p.Ser3579=)
c.6722C= (p.Ser2241=)
c.6698C= (p.Ser2233=)
c.6578C= (p.Ser2193=)
10g.16828833G>TCA376119820CUBNc.10736C>A (p.Ser3579Tyr)
c.6722C>A (p.Ser2241Tyr)
c.6698C>A (p.Ser2233Tyr)
c.6578C>A (p.Ser2193Tyr)
10g.16828834A=CA1893313758CUBNc.10735T= (p.Ser3579=)
c.6721T= (p.Ser2241=)
c.6697T= (p.Ser2233=)
c.6577T= (p.Ser2193=)
10g.16828834A>CCA376119826CUBNc.10735T>G (p.Ser3579Ala)
c.6721T>G (p.Ser2241Ala)
c.6697T>G (p.Ser2233Ala)
c.6577T>G (p.Ser2193Ala)
gnomAD v4
10g.16828834A>GCA376119823CUBNc.10735T>C (p.Ser3579Pro)
c.6721T>C (p.Ser2241Pro)
c.6697T>C (p.Ser2233Pro)
c.6577T>C (p.Ser2193Pro)
10g.16828834A>TCA376119825CUBNc.10735T>A (p.Ser3579Thr)
c.6721T>A (p.Ser2241Thr)
c.6697T>A (p.Ser2233Thr)
c.6577T>A (p.Ser2193Thr)
dbSNP COSMIC
10g.16828835G>ACA468407471CUBNc.10734C>T (p.Ser3578=)
c.6720C>T (p.Ser2240=)
c.6696C>T (p.Ser2232=)
c.6576C>T (p.Ser2192=)
10g.16828835G>CCA376119829CUBNc.10734C>G (p.Ser3578Arg)
c.6720C>G (p.Ser2240Arg)
c.6696C>G (p.Ser2232Arg)
c.6576C>G (p.Ser2192Arg)
gnomAD v4
10g.16828835G>TCA376119831CUBNc.10734C>A (p.Ser3578Arg)
c.6720C>A (p.Ser2240Arg)
c.6696C>A (p.Ser2232Arg)
c.6576C>A (p.Ser2192Arg)
COSMIC
10g.16828836C>ACA376119833CUBNc.10733G>T (p.Ser3578Ile)
c.6719G>T (p.Ser2240Ile)
c.6695G>T (p.Ser2232Ile)
c.6575G>T (p.Ser2192Ile)
10g.16828836C>GCA376119835CUBNc.10733G>C (p.Ser3578Thr)
c.6719G>C (p.Ser2240Thr)
c.6695G>C (p.Ser2232Thr)
c.6575G>C (p.Ser2192Thr)
10g.16828836C>TCA376119837CUBNc.10733G>A (p.Ser3578Asn)
c.6719G>A (p.Ser2240Asn)
c.6695G>A (p.Ser2232Asn)
c.6575G>A (p.Ser2192Asn)
10g.16828836_16828837insAGCA2537494187CUBNc.10732_10733insCT (p.Ser3578ThrfsTer16)
c.6718_6719insCT (p.Ser2240ThrfsTer16)
c.6694_6695insCT (p.Ser2232ThrfsTer16)
c.6574_6575insCT (p.Ser2192ThrfsTer16)
10g.16828837T>ACA376119840CUBNc.10732A>T (p.Ser3578Cys)
c.6718A>T (p.Ser2240Cys)
c.6694A>T (p.Ser2232Cys)
c.6574A>T (p.Ser2192Cys)
10g.16828837T>CCA376119844CUBNc.10732A>G (p.Ser3578Gly)
c.6718A>G (p.Ser2240Gly)
c.6694A>G (p.Ser2232Gly)
c.6574A>G (p.Ser2192Gly)
10g.16828837T>GCA376119842CUBNc.10732A>C (p.Ser3578Arg)
c.6718A>C (p.Ser2240Arg)
c.6694A>C (p.Ser2232Arg)
c.6574A>C (p.Ser2192Arg)
10g.16828838G>ACA468407477CUBNc.10731C>T (p.Ala3577=)
c.6717C>T (p.Ala2239=)
c.6693C>T (p.Ala2231=)
c.6573C>T (p.Ala2191=)
10g.16828838G>CCA468407478CUBNc.10731C>G (p.Ala3577=)
c.6717C>G (p.Ala2239=)
c.6693C>G (p.Ala2231=)
c.6573C>G (p.Ala2191=)
10g.16828838G>TCA468407479CUBNc.10731C>A (p.Ala3577=)
c.6717C>A (p.Ala2239=)
c.6693C>A (p.Ala2231=)
c.6573C>A (p.Ala2191=)
10g.16828839G>ACA376119847CUBNc.10730C>T (p.Ala3577Val)
c.6716C>T (p.Ala2239Val)
c.6692C>T (p.Ala2231Val)
c.6572C>T (p.Ala2191Val)
10g.16828839G>CCA376119848CUBNc.10730C>G (p.Ala3577Gly)
c.6716C>G (p.Ala2239Gly)
c.6692C>G (p.Ala2231Gly)
c.6572C>G (p.Ala2191Gly)
10g.16828839G>TCA376119849CUBNc.10730C>A (p.Ala3577Asp)
c.6716C>A (p.Ala2239Asp)
c.6692C>A (p.Ala2231Asp)
c.6572C>A (p.Ala2191Asp)
10g.16828839_16828840insTGCA2564698317CUBNc.10730_10731insAC (p.Ser3578ProfsTer16)
c.6716_6717insAC (p.Ser2240ProfsTer16)
c.6692_6693insAC (p.Ser2232ProfsTer16)
c.6572_6573insAC (p.Ser2192ProfsTer16)
10g.16828840C>ACA376119850CUBNc.10729G>T (p.Ala3577Ser)
c.6715G>T (p.Ala2239Ser)
c.6691G>T (p.Ala2231Ser)
c.6571G>T (p.Ala2191Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.16828840C=CA1893313765CUBNc.10729G= (p.Ala3577=)
c.6715G= (p.Ala2239=)
c.6691G= (p.Ala2231=)
c.6571G= (p.Ala2191=)
10g.16828840C>GCA376119851CUBNc.10729G>C (p.Ala3577Pro)
c.6715G>C (p.Ala2239Pro)
c.6691G>C (p.Ala2231Pro)
c.6571G>C (p.Ala2191Pro)
10g.16828840C>TCA5422310CUBNc.10729G>A (p.Ala3577Thr)
c.6715G>A (p.Ala2239Thr)
c.6691G>A (p.Ala2231Thr)
c.6571G>A (p.Ala2191Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.16828841G>ACA5422311CUBNc.10728C>T (p.Asn3576=)
c.6714C>T (p.Asn2238=)
c.6690C>T (p.Asn2230=)
c.6570C>T (p.Asn2190=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.16828841G>CCA376119852CUBNc.10728C>G (p.Asn3576Lys)
c.6714C>G (p.Asn2238Lys)
c.6690C>G (p.Asn2230Lys)
c.6570C>G (p.Asn2190Lys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.16828841G=CA1893313775CUBNc.10728C= (p.Asn3576=)
c.6714C= (p.Asn2238=)
c.6690C= (p.Asn2230=)
c.6570C= (p.Asn2190=)

Number of alleles fetched