2 | g.135789601T>A | CA348585998 | LCT | c.5533A>T (p.Thr1845Ser)
| |
2 | g.135789601T>C | CA348585999 | LCT | c.5533A>G (p.Thr1845Ala)
| |
2 | g.135789601T>G | CA348586000 | LCT | c.5533A>C (p.Thr1845Pro)
| |
2 | g.135789602A= | CA1290822665 | LCT | c.5532T= (p.Ala1844=)
| |
2 | g.135789602A>C | CA429084990 | LCT | c.5532T>G (p.Ala1844=)
| |
2 | g.135789602A>G | CA56594950 | LCT | c.5532T>C (p.Ala1844=)
| dbSNP |
2 | g.135789602A>T | CA429084991 | LCT | c.5532T>A (p.Ala1844=)
| |
2 | g.135789603G>A | CA348586002 | LCT | c.5531C>T (p.Ala1844Val)
| |
2 | g.135789603G>C | CA348586003 | LCT | c.5531C>G (p.Ala1844Gly)
| |
2 | g.135789603G>T | CA348586001 | LCT | c.5531C>A (p.Ala1844Asp)
| |
2 | g.135789604C>A | CA348586004 | LCT | c.5530G>T (p.Ala1844Ser)
| |
2 | g.135789604C= | CA1290822666 | LCT | c.5530G= (p.Ala1844=)
| |
2 | g.135789604C>G | CA348586005 | LCT | c.5530G>C (p.Ala1844Pro)
| |
2 | g.135789604C>T | CA348586007 | LCT | c.5530G>A (p.Ala1844Thr)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135789605G>A | CA1887602 | LCT | c.5529C>T (p.Pro1843=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135789605G>C | CA429084995 | LCT | c.5529C>G (p.Pro1843=)
| |
2 | g.135789605G= | CA1290822667 | LCT | c.5529C= (p.Pro1843=)
| |
2 | g.135789605G>T | CA429084996 | LCT | c.5529C>A (p.Pro1843=)
| |
2 | g.135789606G>A | CA348586011 | LCT | c.5528C>T (p.Pro1843Leu)
| |
2 | g.135789606G>C | CA348586013 | LCT | c.5528C>G (p.Pro1843Arg)
| |
2 | g.135789606G>T | CA348586016 | LCT | c.5528C>A (p.Pro1843His)
| dbSNP |
2 | g.135789607G>A | CA348586019 | LCT | c.5527C>T (p.Pro1843Ser)
| |
2 | g.135789607G>C | CA348586022 | LCT | c.5527C>G (p.Pro1843Ala)
| |
2 | g.135789607G>T | CA348586025 | LCT | c.5527C>A (p.Pro1843Thr)
| |
2 | g.135789608G>A | CA429084999 | LCT | c.5526C>T (p.Asp1842=)
| |
2 | g.135789608G>C | CA348586029 | LCT | c.5526C>G (p.Asp1842Glu)
| |
2 | g.135789608G>T | CA348586031 | LCT | c.5526C>A (p.Asp1842Glu)
| |
2 | g.135789609T>A | CA348586036 | LCT | c.5525A>T (p.Asp1842Val)
| |
2 | g.135789609T>C | CA348586038 | LCT | c.5525A>G (p.Asp1842Gly)
| |
2 | g.135789609T>G | CA1887603 | LCT | c.5525A>C (p.Asp1842Ala)
| dbSNP ExAC gnomAD v2 |
2 | g.135789609T= | CA1290822668 | LCT | c.5525A= (p.Asp1842=)
| |
2 | g.135789610C>A | CA348586041 | LCT | c.5524G>T (p.Asp1842Tyr)
| |
2 | g.135789610C>G | CA348586044 | LCT | c.5524G>C (p.Asp1842His)
| |
2 | g.135789610C>T | CA348586046 | LCT | c.5524G>A (p.Asp1842Asn)
| |
2 | g.135789611A>C | CA429085003 | LCT | c.5523T>G (p.Pro1841=)
| |
2 | g.135789611A>G | CA429085004 | LCT | c.5523T>C (p.Pro1841=)
| |
2 | g.135789611A>T | CA429085005 | LCT | c.5523T>A (p.Pro1841=)
| |
2 | g.135789612G>A | CA348586050 | LCT | c.5522C>T (p.Pro1841Leu)
| |
2 | g.135789612G>C | CA348586052 | LCT | c.5522C>G (p.Pro1841Arg)
| |
2 | g.135789612G>T | CA348586054 | LCT | c.5522C>A (p.Pro1841His)
| |
2 | g.135789613G>A | CA348586058 | LCT | c.5521C>T (p.Pro1841Ser)
| |
2 | g.135789613G>C | CA348586063 | LCT | c.5521C>G (p.Pro1841Ala)
| |
2 | g.135789613G>T | CA348586060 | LCT | c.5521C>A (p.Pro1841Thr)
| |
2 | g.135789614G>A | CA429085007 | LCT | c.5520C>T (p.Phe1840=)
| gnomAD v4 |
2 | g.135789614G>C | CA348586067 | LCT | c.5520C>G (p.Phe1840Leu)
| |
2 | g.135789614G>T | CA348586069 | LCT | c.5520C>A (p.Phe1840Leu)
| |
2 | g.135789615A>C | CA348586073 | LCT | c.5519T>G (p.Phe1840Cys)
| |
2 | g.135789615A>G | CA348586075 | LCT | c.5519T>C (p.Phe1840Ser)
| |
2 | g.135789615A>T | CA348586077 | LCT | c.5519T>A (p.Phe1840Tyr)
| |
2 | g.135789616A>C | CA348586086 | LCT | c.5518T>G (p.Phe1840Val)
| |
2 | g.135789616A>G | CA348586083 | LCT | c.5518T>C (p.Phe1840Leu)
| |
2 | g.135789616A>T | CA348586082 | LCT | c.5518T>A (p.Phe1840Ile)
| |
2 | g.135789617G>A | CA429085010 | LCT | c.5517C>T (p.Gly1839=)
| |
2 | g.135789617G>C | CA429085011 | LCT | c.5517C>G (p.Gly1839=)
| |
2 | g.135789617G>T | CA429085013 | LCT | c.5517C>A (p.Gly1839=)
| |
2 | g.135789618C>A | CA348586090 | LCT | c.5516G>T (p.Gly1839Val)
| |
2 | g.135789618C= | CA1290822669 | LCT | c.5516G= (p.Gly1839=)
| |
2 | g.135789618C>G | CA348586089 | LCT | c.5516G>C (p.Gly1839Ala)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135789618C>T | CA1887604 | LCT | c.5516G>A (p.Gly1839Asp)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135789619C>A | CA348586095 | LCT | c.5515G>T (p.Gly1839Cys)
| |
2 | g.135789619C>G | CA348586099 | LCT | c.5515G>C (p.Gly1839Arg)
| |
2 | g.135789619C>T | CA348586097 | LCT | c.5515G>A (p.Gly1839Ser)
| |
2 | g.135789620del | CA2697551029 | LCT | c.5514del (p.Asn1838LysfsTer26)
| ClinVar |
2 | g.135789620A>C | CA348586103 | LCT | c.5514T>G (p.Asn1838Lys)
| |
2 | g.135789620A>G | CA429085017 | LCT | c.5514T>C (p.Asn1838=)
| gnomAD v4 |
2 | g.135789620A>T | CA348586105 | LCT | c.5514T>A (p.Asn1838Lys)
| |
2 | g.135789621T>A | CA348586109 | LCT | c.5513A>T (p.Asn1838Ile)
| |
2 | g.135789621T>C | CA348586111 | LCT | c.5513A>G (p.Asn1838Ser)
| dbSNP gnomAD v4 |
2 | g.135789621T>G | CA348586113 | LCT | c.5513A>C (p.Asn1838Thr)
| |
2 | g.135789621T= | CA1290822670 | LCT | c.5513A= (p.Asn1838=)
| |
2 | g.135789622T>A | CA348586117 | LCT | c.5512A>T (p.Asn1838Tyr)
| |
2 | g.135789622T>C | CA348586119 | LCT | c.5512A>G (p.Asn1838Asp)
| |
2 | g.135789622T>G | CA348586120 | LCT | c.5512A>C (p.Asn1838His)
| |
2 | g.135789623G>A | CA429085019 | LCT | c.5511C>T (p.Cys1837=)
| ClinVar |
2 | g.135789623G>C | CA348586122 | LCT | c.5511C>G (p.Cys1837Trp)
| |
2 | g.135789623G>T | CA348586124 | LCT | c.5511C>A (p.Cys1837Ter)
| |
2 | g.135789624C>A | CA348586127 | LCT | c.5510G>T (p.Cys1837Phe)
| |
2 | g.135789624C>G | CA348586129 | LCT | c.5510G>C (p.Cys1837Ser)
| |
2 | g.135789624C>T | CA348586132 | LCT | c.5510G>A (p.Cys1837Tyr)
| |
2 | g.135789625A>C | CA348586135 | LCT | c.5509T>G (p.Cys1837Gly)
| |
2 | g.135789625A>G | CA348586140 | LCT | c.5509T>C (p.Cys1837Arg)
| |
2 | g.135789625A>T | CA348586137 | LCT | c.5509T>A (p.Cys1837Ser)
| |
2 | g.135789626T>A | CA429085021 | LCT | c.5508A>T (p.Arg1836=)
| |
2 | g.135789626T>C | CA429085022 | LCT | c.5508A>G (p.Arg1836=)
| |
2 | g.135789626T>G | CA429085023 | LCT | c.5508A>C (p.Arg1836=)
| |
2 | g.135789627C>A | CA348586144 | LCT | c.5507G>T (p.Arg1836Leu)
| |
2 | g.135789627C= | CA1290822671 | LCT | c.5507G= (p.Arg1836=)
| |
2 | g.135789627C>G | CA348586146 | LCT | c.5507G>C (p.Arg1836Pro)
| |
2 | g.135789627C>T | CA348586148 | LCT | c.5507G>A (p.Arg1836Gln)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135789628G>A | CA348586150 | LCT | c.5506C>T (p.Arg1836Ter)
| gnomAD v4 COSMIC |
2 | g.135789628G>C | CA348586153 | LCT | c.5506C>G (p.Arg1836Gly)
| |
2 | g.135789628G>T | CA429085024 | LCT | c.5506C>A (p.Arg1836=)
| COSMIC |
2 | g.135789629G>A | CA1887605 | LCT | c.5505C>T (p.Val1835=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135789629G>C | CA429085026 | LCT | c.5505C>G (p.Val1835=)
| |
2 | g.135789629G= | CA1290822672 | LCT | c.5505C= (p.Val1835=)
| |
2 | g.135789629G>T | CA429085025 | LCT | c.5505C>A (p.Val1835=)
| |
2 | g.135789630A>C | CA348586159 | LCT | c.5504T>G (p.Val1835Gly)
| |
2 | g.135789630A>G | CA348586161 | LCT | c.5504T>C (p.Val1835Ala)
| |
2 | g.135789630A>T | CA348586164 | LCT | c.5504T>A (p.Val1835Asp)
| |
2 | g.135789631C>A | CA348586172 | LCT | c.5503G>T (p.Val1835Phe)
| |
2 | g.135789631C>G | CA348586170 | LCT | c.5503G>C (p.Val1835Leu)
| |
2 | g.135789631C>T | CA348586168 | LCT | c.5503G>A (p.Val1835Ile)
| |
2 | g.135789632C>A | CA429085027 | LCT | c.5502G>T (p.Val1834=)
| |
2 | g.135789632C= | CA1290822673 | LCT | c.5502G= (p.Val1834=)
| |
2 | g.135789632C>G | CA429085028 | LCT | c.5502G>C (p.Val1834=)
| |
2 | g.135789632C>T | CA56594976 | LCT | c.5502G>A (p.Val1834=)
| dbSNP |
2 | g.135789633A>C | CA348586177 | LCT | c.5501T>G (p.Val1834Gly)
| |
2 | g.135789633A>G | CA348586179 | LCT | c.5501T>C (p.Val1834Ala)
| |
2 | g.135789633A>T | CA348586181 | LCT | c.5501T>A (p.Val1834Glu)
| |
2 | g.135789634C>A | CA348586184 | LCT | c.5500G>T (p.Val1834Leu)
| |
2 | g.135789634C= | CA1290822674 | LCT | c.5500G= (p.Val1834=)
| |
2 | g.135789634C>G | CA348586186 | LCT | c.5500G>C (p.Val1834Leu)
| |
2 | g.135789634C>T | CA348586187 | LCT | c.5500G>A (p.Val1834Met)
| dbSNP |
2 | g.135789635A>C | CA429085032 | LCT | c.5499T>G (p.Ser1833=)
| |
2 | g.135789635A>G | CA429085033 | LCT | c.5499T>C (p.Ser1833=)
| gnomAD v4 |
2 | g.135789635A>T | CA429085034 | LCT | c.5499T>A (p.Ser1833=)
| |
2 | g.135789637_135789638del | CA2577107650 | LCT | c.5498_5499del (p.Ser1833CysfsTer9)
| |
2 | g.135789636G>A | CA348586192 | LCT | c.5498C>T (p.Ser1833Phe)
| |
2 | g.135789636G>C | CA348586194 | LCT | c.5498C>G (p.Ser1833Cys)
| |
2 | g.135789636G>T | CA348586196 | LCT | c.5498C>A (p.Ser1833Tyr)
| |
2 | g.135789637A>C | CA348586200 | LCT | c.5497T>G (p.Ser1833Ala)
| |
2 | g.135789637A>G | CA348586202 | LCT | c.5497T>C (p.Ser1833Pro)
| |
2 | g.135789637A>T | CA348586204 | LCT | c.5497T>A (p.Ser1833Thr)
| |
2 | g.135789638G>A | CA56594977 | LCT | c.5496C>T (p.Ala1832=)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135789638G>C | CA429085039 | LCT | c.5496C>G (p.Ala1832=)
| |
2 | g.135789638G= | CA1290822675 | LCT | c.5496C= (p.Ala1832=)
| |
2 | g.135789638G>T | CA429085036 | LCT | c.5496C>A (p.Ala1832=)
| |
2 | g.135789639G>A | CA348586212 | LCT | c.5495C>T (p.Ala1832Val)
| |
2 | g.135789639G>C | CA348586207 | LCT | c.5495C>G (p.Ala1832Gly)
| |
2 | g.135789639G>T | CA348586209 | LCT | c.5495C>A (p.Ala1832Asp)
| |
2 | g.135789641_135789652dup | CA2577107653 | LCT | c.5484_5495dup (p.Ala1832_Ser1833insLysPheTyrAla)
| gnomAD v4 |
2 | g.135789640C>A | CA348586215 | LCT | c.5494G>T (p.Ala1832Ser)
| |
2 | g.135789640C= | CA1290822676 | LCT | c.5494G= (p.Ala1832=)
| |
2 | g.135789640C>G | CA348586217 | LCT | c.5494G>C (p.Ala1832Pro)
| |
2 | g.135789640C>T | CA348586219 | LCT | c.5494G>A (p.Ala1832Thr)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135789641G>A | CA1887606 | LCT | c.5493C>T (p.Tyr1831=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135789641G>C | CA348586224 | LCT | c.5493C>G (p.Tyr1831Ter)
| |
2 | g.135789641G= | CA1290822677 | LCT | c.5493C= (p.Tyr1831=)
| |
2 | g.135789641G>T | CA348586226 | LCT | c.5493C>A (p.Tyr1831Ter)
| |
2 | g.135789642T>A | CA348586230 | LCT | c.5492A>T (p.Tyr1831Phe)
| |
2 | g.135789642T>C | CA1887607 | LCT | c.5492A>G (p.Tyr1831Cys)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135789642T>G | CA348586232 | LCT | c.5492A>C (p.Tyr1831Ser)
| |
2 | g.135789642T= | CA1290822678 | LCT | c.5492A= (p.Tyr1831=)
| |
2 | g.135789643A>C | CA348586235 | LCT | c.5491T>G (p.Tyr1831Asp)
| |
2 | g.135789643A>G | CA348586238 | LCT | c.5491T>C (p.Tyr1831His)
| |
2 | g.135789643A>T | CA348586240 | LCT | c.5491T>A (p.Tyr1831Asn)
| |
2 | g.135789644G>A | CA429085042 | LCT | c.5490C>T (p.Phe1830=)
| |
2 | g.135789644G>C | CA348586246 | LCT | c.5490C>G (p.Phe1830Leu)
| |
2 | g.135789644G>T | CA348586244 | LCT | c.5490C>A (p.Phe1830Leu)
| |
2 | g.135789645A>C | CA348586250 | LCT | c.5489T>G (p.Phe1830Cys)
| |
2 | g.135789645A>G | CA348586253 | LCT | c.5489T>C (p.Phe1830Ser)
| |
2 | g.135789645A>T | CA348586251 | LCT | c.5489T>A (p.Phe1830Tyr)
| |
2 | g.135789646A>C | CA348586256 | LCT | c.5488T>G (p.Phe1830Val)
| |
2 | g.135789646A>G | CA348586259 | LCT | c.5488T>C (p.Phe1830Leu)
| |
2 | g.135789646A>T | CA348586261 | LCT | c.5488T>A (p.Phe1830Ile)
| |
2 | g.135789647C>A | CA348586265 | LCT | c.5487G>T (p.Lys1829Asn)
| COSMIC |
2 | g.135789647C>G | CA348586267 | LCT | c.5487G>C (p.Lys1829Asn)
| |
2 | g.135789647C>T | CA429085046 | LCT | c.5487G>A (p.Lys1829=)
| |
2 | g.135789648T>A | CA348586270 | LCT | c.5486A>T (p.Lys1829Met)
| |
2 | g.135789648T>C | CA1887608 | LCT | c.5486A>G (p.Lys1829Arg)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135789648T>G | CA348586275 | LCT | c.5486A>C (p.Lys1829Thr)
| |
2 | g.135789648T= | CA1290822679 | LCT | c.5486A= (p.Lys1829=)
| |
2 | g.135789649T>A | CA348586278 | LCT | c.5485A>T (p.Lys1829Ter)
| |
2 | g.135789649T>C | CA348586280 | LCT | c.5485A>G (p.Lys1829Glu)
| |
2 | g.135789649T>G | CA348586283 | LCT | c.5485A>C (p.Lys1829Gln)
| |
2 | g.135789650C>A | CA429085051 | LCT | c.5484G>T (p.Ala1828=)
| |
2 | g.135789650C= | CA1290822680 | LCT | c.5484G= (p.Ala1828=)
| |
2 | g.135789650C>G | CA429085052 | LCT | c.5484G>C (p.Ala1828=)
| |
2 | g.135789650C>T | CA1887609 | LCT | c.5484G>A (p.Ala1828=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.135789651G>A | CA1887610 | LCT | c.5483C>T (p.Ala1828Val)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135789651G>C | CA348586292 | LCT | c.5483C>G (p.Ala1828Gly)
| |
2 | g.135789651G= | CA1290822681 | LCT | c.5483C= (p.Ala1828=)
| |
2 | g.135789651G>T | CA348586289 | LCT | c.5483C>A (p.Ala1828Glu)
| |
2 | g.135789652C>A | CA348586297 | LCT | c.5482G>T (p.Ala1828Ser)
| |
2 | g.135789652C= | CA1290822682 | LCT | c.5482G= (p.Ala1828=)
| |
2 | g.135789652C>G | CA348586300 | LCT | c.5482G>C (p.Ala1828Pro)
| |
2 | g.135789652C>T | CA1887611 | LCT | c.5482G>A (p.Ala1828Thr)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135789653T>A | CA429085055 | LCT | c.5481A>T (p.Ser1827=)
| |
2 | g.135789653T>C | CA429085056 | LCT | c.5481A>G (p.Ser1827=)
| |
2 | g.135789653T>G | CA429085058 | LCT | c.5481A>C (p.Ser1827=)
| |
2 | g.135789654G>A | CA348586306 | LCT | c.5480C>T (p.Ser1827Leu)
| |
2 | g.135789654G>C | CA348586308 | LCT | c.5480C>G (p.Ser1827Ter)
| |
2 | g.135789654G>T | CA348586310 | LCT | c.5480C>A (p.Ser1827Ter)
| |
2 | g.135789655A>C | CA348586314 | LCT | c.5479T>G (p.Ser1827Ala)
| |
2 | g.135789655A>G | CA348586317 | LCT | c.5479T>C (p.Ser1827Pro)
| |
2 | g.135789655A>T | CA348586319 | LCT | c.5479T>A (p.Ser1827Thr)
| |
2 | g.135789656T>A | CA429085059 | LCT | c.5478A>T (p.Ala1826=)
| |
2 | g.135789656T>C | CA56595009 | LCT | c.5478A>G (p.Ala1826=)
| dbSNP gnomAD v4 |
2 | g.135789656T>G | CA429085060 | LCT | c.5478A>C (p.Ala1826=)
| |
2 | g.135789656T= | CA1290822683 | LCT | c.5478A= (p.Ala1826=)
| |
2 | g.135789657G>A | CA348586321 | LCT | c.5477C>T (p.Ala1826Val)
| |
2 | g.135789657G>C | CA348586324 | LCT | c.5477C>G (p.Ala1826Gly)
| |
2 | g.135789657G>T | CA348586326 | LCT | c.5477C>A (p.Ala1826Glu)
| |
2 | g.135789658del | CA2661273565 | LCT | c.5476del (p.Ala1826HisfsTer?)
| gnomAD v4 |
2 | g.135789658C>A | CA348586336 | LCT | c.5476G>T (p.Ala1826Ser)
| |
2 | g.135789658C>G | CA348586333 | LCT | c.5476G>C (p.Ala1826Pro)
| |
2 | g.135789658C>T | CA348586331 | LCT | c.5476G>A (p.Ala1826Thr)
| |
2 | g.135789659T>A | CA348586340 | LCT | c.5475A>T (p.Lys1825Asn)
| |
2 | g.135789659T>C | CA429085061 | LCT | c.5475A>G (p.Lys1825=)
| |
2 | g.135789659T>G | CA348586342 | LCT | c.5475A>C (p.Lys1825Asn)
| |
2 | g.135789660T>A | CA348586344 | LCT | c.5474A>T (p.Lys1825Ile)
| |
2 | g.135789660T>C | CA348586347 | LCT | c.5474A>G (p.Lys1825Arg)
| |
2 | g.135789660T>G | CA348586349 | LCT | c.5474A>C (p.Lys1825Thr)
| |
2 | g.135789661T>A | CA348586354 | LCT | c.5473A>T (p.Lys1825Ter)
| |
2 | g.135789661T>C | CA348586356 | LCT | c.5473A>G (p.Lys1825Glu)
| gnomAD v4 |
2 | g.135789661T>G | CA348586359 | LCT | c.5473A>C (p.Lys1825Gln)
| |
2 | g.135789662G>A | CA429085064 | LCT | c.5472C>T (p.Pro1824=)
| |
2 | g.135789662G>C | CA429085065 | LCT | c.5472C>G (p.Pro1824=)
| |
2 | g.135789662G>T | CA429085066 | LCT | c.5472C>A (p.Pro1824=)
| gnomAD v4 |
2 | g.135789663G>A | CA348586363 | LCT | c.5471C>T (p.Pro1824Leu)
| |
2 | g.135789663G>C | CA348586365 | LCT | c.5471C>G (p.Pro1824Arg)
| |
2 | g.135789663G>T | CA348586367 | LCT | c.5471C>A (p.Pro1824His)
| |
2 | g.135789664G>A | CA348586370 | LCT | c.5470C>T (p.Pro1824Ser)
| |
2 | g.135789664G>C | CA348586372 | LCT | c.5470C>G (p.Pro1824Ala)
| |
2 | g.135789664G>T | CA348586374 | LCT | c.5470C>A (p.Pro1824Thr)
| |
2 | g.135789665G>A | CA429085067 | LCT | c.5469C>T (p.Ile1823=)
| gnomAD v4 |
2 | g.135789665G>C | CA348586377 | LCT | c.5469C>G (p.Ile1823Met)
| |
2 | g.135789665G>T | CA429085068 | LCT | c.5469C>A (p.Ile1823=)
| COSMIC |
2 | g.135789666A>C | CA348586380 | LCT | c.5468T>G (p.Ile1823Ser)
| |
2 | g.135789666A>G | CA348586382 | LCT | c.5468T>C (p.Ile1823Thr)
| |
2 | g.135789666A>T | CA348586386 | LCT | c.5468T>A (p.Ile1823Asn)
| |
2 | g.135789667T>A | CA348586389 | LCT | c.5467A>T (p.Ile1823Phe)
| |
2 | g.135789667T>C | CA348586392 | LCT | c.5467A>G (p.Ile1823Val)
| dbSNP |
2 | g.135789667T>G | CA348586393 | LCT | c.5467A>C (p.Ile1823Leu)
| |
2 | g.135789667T= | CA1290822684 | LCT | c.5467A= (p.Ile1823=)
| |
2 | g.135789668C>A | CA348586397 | LCT | c.5466G>T (p.Arg1822Ser)
| |
2 | g.135789668C= | CA1290822685 | LCT | c.5466G= (p.Arg1822=)
| |
2 | g.135789668C>G | CA348586400 | LCT | c.5466G>C (p.Arg1822Ser)
| |
2 | g.135789668C>T | CA56595012 | LCT | c.5466G>A (p.Arg1822=)
| dbSNP |
2 | g.135789669C>A | CA348586404 | LCT | c.5465G>T (p.Arg1822Met)
| |
2 | g.135789669C>G | CA348586407 | LCT | c.5465G>C (p.Arg1822Thr)
| |
2 | g.135789669C>T | CA348586410 | LCT | c.5465G>A (p.Arg1822Lys)
| |
2 | g.135789670T>A | CA348586412 | LCT | c.5464A>T (p.Arg1822Trp)
| |
2 | g.135789670T>C | CA348586414 | LCT | c.5464A>G (p.Arg1822Gly)
| COSMIC |
2 | g.135789670T>G | CA429085069 | LCT | c.5464A>C (p.Arg1822=)
| |
2 | g.135789671T>A | CA429085070 | LCT | c.5463A>T (p.Pro1821=)
| |
2 | g.135789671T>C | CA429085071 | LCT | c.5463A>G (p.Pro1821=)
| |
2 | g.135789671T>G | CA429085072 | LCT | c.5463A>C (p.Pro1821=)
| |
2 | g.135789672G>A | CA348586420 | LCT | c.5462C>T (p.Pro1821Leu)
| |
2 | g.135789672G>C | CA348586423 | LCT | c.5462C>G (p.Pro1821Arg)
| |
2 | g.135789672G>T | CA348586418 | LCT | c.5462C>A (p.Pro1821Gln)
| |
2 | g.135789673G>A | CA348586426 | LCT | c.5461C>T (p.Pro1821Ser)
| gnomAD v4 |
2 | g.135789673G>C | CA348586428 | LCT | c.5461C>G (p.Pro1821Ala)
| |
2 | g.135789673G>T | CA348586427 | LCT | c.5461C>A (p.Pro1821Thr)
| |
2 | g.135789674C>A | CA429085073 | LCT | c.5460G>T (p.Leu1820=)
| |
2 | g.135789674C= | CA1290822686 | LCT | c.5460G= (p.Leu1820=)
| |
2 | g.135789674C>G | CA429085074 | LCT | c.5460G>C (p.Leu1820=)
| |
2 | g.135789674C>T | CA1887612 | LCT | c.5460G>A (p.Leu1820=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135789675A>C | CA348586430 | LCT | c.5459T>G (p.Leu1820Arg)
| ClinVar |
2 | g.135789675A>G | CA348586429 | LCT | c.5459T>C (p.Leu1820Pro)
| |
2 | g.135789675A>T | CA348586431 | LCT | c.5459T>A (p.Leu1820Gln)
| |
2 | g.135789676G>A | CA429085075 | LCT | c.5458C>T (p.Leu1820=)
| |
2 | g.135789676G>C | CA348586432 | LCT | c.5458C>G (p.Leu1820Val)
| |
2 | g.135789676G>T | CA348586433 | LCT | c.5458C>A (p.Leu1820Met)
| |
2 | g.135789677A>C | CA429085076 | LCT | c.5457T>G (p.Ser1819=)
| |
2 | g.135789677A>G | CA429085077 | LCT | c.5457T>C (p.Ser1819=)
| |
2 | g.135789677A>T | CA429085078 | LCT | c.5457T>A (p.Ser1819=)
| |
2 | g.135789678G>A | CA348586434 | LCT | c.5456C>T (p.Ser1819Phe)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135789678G>C | CA348586435 | LCT | c.5456C>G (p.Ser1819Cys)
| |
2 | g.135789678G= | CA1290822687 | LCT | c.5456C= (p.Ser1819=)
| |
2 | g.135789678G>T | CA348586436 | LCT | c.5456C>A (p.Ser1819Tyr)
| |
2 | g.135789679A>C | CA348586437 | LCT | c.5455T>G (p.Ser1819Ala)
| |
2 | g.135789679A>G | CA348586438 | LCT | c.5455T>C (p.Ser1819Pro)
| |
2 | g.135789679A>T | CA348586439 | LCT | c.5455T>A (p.Ser1819Thr)
| |
2 | g.135789680A= | CA1290822688 | LCT | c.5454T= (p.Pro1818=)
| |
2 | g.135789680A>C | CA429085079 | LCT | c.5454T>G (p.Pro1818=)
| |
2 | g.135789680A>G | CA56595046 | LCT | c.5454T>C (p.Pro1818=)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135789680A>T | CA429085080 | LCT | c.5454T>A (p.Pro1818=)
| |
2 | g.135789681G>A | CA348586440 | LCT | c.5453C>T (p.Pro1818Leu)
| |
2 | g.135789681G>C | CA348586441 | LCT | c.5453C>G (p.Pro1818Arg)
| COSMIC |
2 | g.135789681G>T | CA348586442 | LCT | c.5453C>A (p.Pro1818His)
| dbSNP |
2 | g.135789682G>A | CA348586445 | LCT | c.5452C>T (p.Pro1818Ser)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135789682G>C | CA348586443 | LCT | c.5452C>G (p.Pro1818Ala)
| |
2 | g.135789682G= | CA1290822689 | LCT | c.5452C= (p.Pro1818=)
| |
2 | g.135789682G>T | CA348586444 | LCT | c.5452C>A (p.Pro1818Thr)
| |
2 | g.135789683G>A | CA429085081 | LCT | c.5451C>T (p.Asp1817=)
| |
2 | g.135789683G>C | CA348586446 | LCT | c.5451C>G (p.Asp1817Glu)
| dbSNP |
2 | g.135789683G= | CA1290822690 | LCT | c.5451C= (p.Asp1817=)
| |
2 | g.135789683G>T | CA348586447 | LCT | c.5451C>A (p.Asp1817Glu)
| dbSNP |
2 | g.135789684T>A | CA348586448 | LCT | c.5450A>T (p.Asp1817Val)
| |
2 | g.135789684T>C | CA348586449 | LCT | c.5450A>G (p.Asp1817Gly)
| |
2 | g.135789684T>G | CA348586450 | LCT | c.5450A>C (p.Asp1817Ala)
| |
2 | g.135789685C>A | CA348586451 | LCT | c.5449G>T (p.Asp1817Tyr)
| |
2 | g.135789685C>G | CA348586452 | LCT | c.5449G>C (p.Asp1817His)
| gnomAD v4 |
2 | g.135789685C>T | CA348586453 | LCT | c.5449G>A (p.Asp1817Asn)
| |
2 | g.135789686A>C | CA348586454 | LCT | c.5448T>G (p.Ser1816Arg)
| ClinVar dbSNP |
2 | g.135789686A>G | CA429085082 | LCT | c.5448T>C (p.Ser1816=)
| |
2 | g.135789686A>T | CA348586455 | LCT | c.5448T>A (p.Ser1816Arg)
| |
2 | g.135789687C>A | CA348586457 | LCT | c.5447G>T (p.Ser1816Ile)
| |
2 | g.135789687C= | CA1290822691 | LCT | c.5447G= (p.Ser1816=)
| |
2 | g.135789687C>G | CA1887613 | LCT | c.5447G>C (p.Ser1816Thr)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135789687C>T | CA348586456 | LCT | c.5447G>A (p.Ser1816Asn)
| gnomAD v4 |
2 | g.135789688T>A | CA348586458 | LCT | c.5446A>T (p.Ser1816Cys)
| |
2 | g.135789688T>C | CA348586459 | LCT | c.5446A>G (p.Ser1816Gly)
| gnomAD v4 |
2 | g.135789688T>G | CA348586460 | LCT | c.5446A>C (p.Ser1816Arg)
| |
2 | g.135789689G>A | CA429085083 | LCT | c.5445C>T (p.Tyr1815=)
| |
2 | g.135789689G>C | CA348586461 | LCT | c.5445C>G (p.Tyr1815Ter)
| |
2 | g.135789689G>T | CA348586462 | LCT | c.5445C>A (p.Tyr1815Ter)
| |
2 | g.135789690T>A | CA348586463 | LCT | c.5444A>T (p.Tyr1815Phe)
| |
2 | g.135789690T>C | CA348586464 | LCT | c.5444A>G (p.Tyr1815Cys)
| gnomAD v4 |
2 | g.135789690T>G | CA348586465 | LCT | c.5444A>C (p.Tyr1815Ser)
| |
2 | g.135789691A>C | CA348586466 | LCT | c.5443T>G (p.Tyr1815Asp)
| |
2 | g.135789691A>G | CA348586467 | LCT | c.5443T>C (p.Tyr1815His)
| |
2 | g.135789691A>T | CA348586468 | LCT | c.5443T>A (p.Tyr1815Asn)
| |
2 | g.135789692G>A | CA429085084 | LCT | c.5442C>T (p.Asn1814=)
| |
2 | g.135789692G>C | CA348586469 | LCT | c.5442C>G (p.Asn1814Lys)
| |
2 | g.135789692G>T | CA348586470 | LCT | c.5442C>A (p.Asn1814Lys)
| |
2 | g.135789693T>A | CA348586471 | LCT | c.5441A>T (p.Asn1814Ile)
| |
2 | g.135789693T>C | CA348586473 | LCT | c.5441A>G (p.Asn1814Ser)
| |
2 | g.135789693T>G | CA348586472 | LCT | c.5441A>C (p.Asn1814Thr)
| |
2 | g.135789694T>A | CA348586474 | LCT | c.5440A>T (p.Asn1814Tyr)
| |
2 | g.135789694T>C | CA348586475 | LCT | c.5440A>G (p.Asn1814Asp)
| gnomAD v4 |
2 | g.135789694T>G | CA348586476 | LCT | c.5440A>C (p.Asn1814His)
| |
2 | g.135789695C>A | CA429085085 | LCT | c.5439G>T (p.Val1813=)
| |
2 | g.135789695C= | CA1290822692 | LCT | c.5439G= (p.Val1813=)
| |
2 | g.135789695C>G | CA429085087 | LCT | c.5439G>C (p.Val1813=)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135789695C>T | CA429085086 | LCT | c.5439G>A (p.Val1813=)
| |
2 | g.135789696A>C | CA348586477 | LCT | c.5438T>G (p.Val1813Gly)
| |
2 | g.135789696A>G | CA348586478 | LCT | c.5438T>C (p.Val1813Ala)
| |
2 | g.135789696A>T | CA348586479 | LCT | c.5438T>A (p.Val1813Glu)
| |
2 | g.135789697C>A | CA348586480 | LCT | c.5437G>T (p.Val1813Leu)
| |
2 | g.135789697C>G | CA348586481 | LCT | c.5437G>C (p.Val1813Leu)
| |
2 | g.135789697C>T | CA348586482 | LCT | c.5437G>A (p.Val1813Met)
| |
2 | g.135789698A>C | CA348586483 | LCT | c.5436T>G (p.Phe1812Leu)
| |
2 | g.135789698A>G | CA429085088 | LCT | c.5436T>C (p.Phe1812=)
| gnomAD v4 |
2 | g.135789698A>T | CA348586484 | LCT | c.5436T>A (p.Phe1812Leu)
| |
2 | g.135789699A>C | CA348586486 | LCT | c.5435T>G (p.Phe1812Cys)
| |
2 | g.135789699A>G | CA348586489 | LCT | c.5435T>C (p.Phe1812Ser)
| |
2 | g.135789699A>T | CA348586485 | LCT | c.5435T>A (p.Phe1812Tyr)
| |
2 | g.135789700A= | CA1290822693 | LCT | c.5434T= (p.Phe1812=)
| |
2 | g.135789700A>C | CA348586498 | LCT | c.5434T>G (p.Phe1812Val)
| |
2 | g.135789700A>G | CA348586493 | LCT | c.5434T>C (p.Phe1812Leu)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135789700A>T | CA56595050 | LCT | c.5434T>A (p.Phe1812Ile)
| dbSNP |
2 | g.135789701A= | CA1290822694 | LCT | c.5433T= (p.His1811=)
| |
2 | g.135789701A>C | CA1887614 | LCT | c.5433T>G (p.His1811Gln)
| dbSNP ExAC gnomAD v2 |
2 | g.135789701A>G | CA56595063 | LCT | c.5433T>C (p.His1811=)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135789701A>T | CA348586500 | LCT | c.5433T>A (p.His1811Gln)
| |