UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.75727759C>A | CA401039029 | ITGB4 | c.373C>A (p.Pro125Thr) n.438C>A n.373C>A c.478C>A (p.Pro160Thr) | |
| 17 | g.75727759C= | CA2275653871 | ITGB4 | c.373C= (p.Pro125=) n.438C= n.373C= c.478C= (p.Pro160=) | |
| 17 | g.75727759C>G | CA401039030 | ITGB4 | c.373C>G (p.Pro125Ala) n.438C>G n.373C>G c.478C>G (p.Pro160Ala) | |
| 17 | g.75727759C>T | CA401039031 | ITGB4 | c.373C>T (p.Pro125Ser) n.438C>T n.373C>T c.478C>T (p.Pro160Ser) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.75727760C>A | CA401039032 | ITGB4 | c.374C>A (p.Pro125Gln) n.439C>A n.374C>A c.479C>A (p.Pro160Gln) | |
| 17 | g.75727760C>G | CA401039033 | ITGB4 | c.374C>G (p.Pro125Arg) n.439C>G n.374C>G c.479C>G (p.Pro160Arg) | |
| 17 | g.75727760C>T | CA401039034 | ITGB4 | c.374C>T (p.Pro125Leu) n.439C>T n.374C>T c.479C>T (p.Pro160Leu) | |
| 17 | g.75727761A>C | CA501832185 | ITGB4 | c.375A>C (p.Pro125=) n.440A>C n.375A>C c.480A>C (p.Pro160=) | |
| 17 | g.75727761A>G | CA501832186 | ITGB4 | c.375A>G (p.Pro125=) n.440A>G n.375A>G c.480A>G (p.Pro160=) | |
| 17 | g.75727761A>T | CA501832187 | ITGB4 | c.375A>T (p.Pro125=) n.440A>T n.375A>T c.480A>T (p.Pro160=) | |
| 17 | g.75727762C>A | CA401039035 | ITGB4 | c.376C>A (p.Leu126Met) n.441C>A n.376C>A c.481C>A (p.Leu161Met) | |
| 17 | g.75727762C= | CA2275653872 | ITGB4 | c.376C= (p.Leu126=) n.441C= n.376C= c.481C= (p.Leu161=) | |
| 17 | g.75727762C>G | CA401039036 | ITGB4 | c.376C>G (p.Leu126Val) n.441C>G n.376C>G c.481C>G (p.Leu161Val) | |
| 17 | g.75727762C>T | CA501832188 | ITGB4 | c.376C>T (p.Leu126=) n.441C>T n.376C>T c.481C>T (p.Leu161=) | dbSNP |
| 17 | g.75727763T>A | CA401039037 | ITGB4 | c.377T>A (p.Leu126Gln) n.442T>A n.377T>A c.482T>A (p.Leu161Gln) | |
| 17 | g.75727763T>C | CA401039038 | ITGB4 | c.377T>C (p.Leu126Pro) n.442T>C n.377T>C c.482T>C (p.Leu161Pro) | |
| 17 | g.75727763T>G | CA401039039 | ITGB4 | c.377T>G (p.Leu126Arg) n.442T>G n.377T>G c.482T>G (p.Leu161Arg) | |
| 17 | g.75727764G>A | CA501832191 | ITGB4 | c.378G>A (p.Leu126=) n.443G>A n.378G>A c.483G>A (p.Leu161=) | |
| 17 | g.75727764G>C | CA501832190 | ITGB4 | c.378G>C (p.Leu126=) n.443G>C n.378G>C c.483G>C (p.Leu161=) | |
| 17 | g.75727764G>T | CA501832189 | ITGB4 | c.378G>T (p.Leu126=) n.443G>T n.378G>T c.483G>T (p.Leu161=) | |
| 17 | g.75727765G>A | CA401039040 | ITGB4 | c.379G>A (p.Glu127Lys) n.444G>A n.379G>A c.484G>A (p.Glu162Lys) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.75727765G>C | CA401039042 | ITGB4 | c.379G>C (p.Glu127Gln) n.444G>C n.379G>C c.484G>C (p.Glu162Gln) | |
| 17 | g.75727765G= | CA2275653873 | ITGB4 | c.379G= (p.Glu127=) n.444G= n.379G= c.484G= (p.Glu162=) | |
| 17 | g.75727765G>T | CA401039041 | ITGB4 | c.379G>T (p.Glu127Ter) n.444G>T n.379G>T c.484G>T (p.Glu162Ter) | |
| 17 | g.75727766A>C | CA401039043 | ITGB4 | c.380A>C (p.Glu127Ala) n.445A>C n.380A>C c.485A>C (p.Glu162Ala) | |
| 17 | g.75727766A>G | CA401039044 | ITGB4 | c.380A>G (p.Glu127Gly) n.445A>G n.380A>G c.485A>G (p.Glu162Gly) | |
| 17 | g.75727766A>T | CA401039045 | ITGB4 | c.380A>T (p.Glu127Val) n.445A>T n.380A>T c.485A>T (p.Glu162Val) | |
| 17 | g.75727767G>A | CA501832192 | ITGB4 | c.381G>A (p.Glu127=) n.446G>A n.381G>A c.486G>A (p.Glu162=) | |
| 17 | g.75727767G>C | CA401039046 | ITGB4 | c.381G>C (p.Glu127Asp) n.446G>C n.381G>C c.486G>C (p.Glu162Asp) | |
| 17 | g.75727767G>T | CA401039047 | ITGB4 | c.381G>T (p.Glu127Asp) n.446G>T n.381G>T c.486G>T (p.Glu162Asp) | |
| 17 | g.75727768A>C | CA401039048 | ITGB4 | c.382A>C (p.Ser128Arg) n.447A>C n.382A>C c.487A>C (p.Ser163Arg) | |
| 17 | g.75727768A>G | CA401039049 | ITGB4 | c.382A>G (p.Ser128Gly) n.447A>G n.382A>G c.487A>G (p.Ser163Gly) | |
| 17 | g.75727768A>T | CA401039050 | ITGB4 | c.382A>T (p.Ser128Cys) n.447A>T n.382A>T c.487A>T (p.Ser163Cys) | gnomAD v4 |
| 17 | g.75727769G>A | CA401039051 | ITGB4 | c.383G>A (p.Ser128Asn) n.448G>A n.383G>A c.488G>A (p.Ser163Asn) | |
| 17 | g.75727769G>C | CA401039052 | ITGB4 | c.383G>C (p.Ser128Thr) n.448G>C n.383G>C c.488G>C (p.Ser163Thr) | |
| 17 | g.75727769G>T | CA401039053 | ITGB4 | c.383G>T (p.Ser128Ile) n.448G>T n.383G>T c.488G>T (p.Ser163Ile) | |
| 17 | g.75727770C>A | CA401039055 | ITGB4 | c.384C>A (p.Ser128Arg) n.449C>A n.384C>A c.489C>A (p.Ser163Arg) | |
| 17 | g.75727770C>G | CA401039054 | ITGB4 | c.384C>G (p.Ser128Arg) n.449C>G n.384C>G c.489C>G (p.Ser163Arg) | |
| 17 | g.75727770C>T | CA501832193 | ITGB4 | c.384C>T (p.Ser128=) n.449C>T n.384C>T c.489C>T (p.Ser163=) | |
| 17 | g.75727773del | CA2639874240 | ITGB4 | c.387del (p.Val130TrpfsTer?) n.452del n.387del c.492del (p.Val165TrpfsTer?) | gnomAD v4 |
| 17 | g.75727771C>A | CA401039056 | ITGB4 | c.385C>A (p.Pro129Thr) n.450C>A n.385C>A c.490C>A (p.Pro164Thr) | |
| 17 | g.75727771C= | CA2275653874 | ITGB4 | c.385C= (p.Pro129=) n.450C= n.385C= c.490C= (p.Pro164=) | |
| 17 | g.75727771C>G | CA294058647 | ITGB4 | c.385C>G (p.Pro129Ala) n.450C>G n.385C>G c.490C>G (p.Pro164Ala) | dbSNP |
| 17 | g.75727771C>T | CA401039057 | ITGB4 | c.385C>T (p.Pro129Ser) n.450C>T n.385C>T c.490C>T (p.Pro164Ser) | |
| 17 | g.75727772C>A | CA401039058 | ITGB4 | c.386C>A (p.Pro129His) n.451C>A n.386C>A c.491C>A (p.Pro164His) | |
| 17 | g.75727772C>G | CA401039059 | ITGB4 | c.386C>G (p.Pro129Arg) n.451C>G n.386C>G c.491C>G (p.Pro164Arg) | |
| 17 | g.75727772C>T | CA401039060 | ITGB4 | c.386C>T (p.Pro129Leu) n.451C>T n.386C>T c.491C>T (p.Pro164Leu) | |
| 17 | g.75727773C>A | CA501832194 | ITGB4 | c.387C>A (p.Pro129=) n.452C>A n.387C>A c.492C>A (p.Pro164=) | |
| 17 | g.75727773C= | CA2275653875 | ITGB4 | c.387C= (p.Pro129=) n.452C= n.387C= c.492C= (p.Pro164=) | |
| 17 | g.75727773C>G | CA501832195 | ITGB4 | c.387C>G (p.Pro129=) n.452C>G n.387C>G c.492C>G (p.Pro164=) | gnomAD v4 |
| 17 | g.75727773C>T | CA8768654 | ITGB4 | c.387C>T (p.Pro129=) n.452C>T n.387C>T c.492C>T (p.Pro164=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727774G>A | CA8768655 | ITGB4 | c.388G>A (p.Val130Met) n.453G>A n.388G>A c.493G>A (p.Val165Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727774G>C | CA401039061 | ITGB4 | c.388G>C (p.Val130Leu) n.453G>C n.388G>C c.493G>C (p.Val165Leu) | |
| 17 | g.75727774G= | CA2275653876 | ITGB4 | c.388G= (p.Val130=) n.453G= n.388G= c.493G= (p.Val165=) | |
| 17 | g.75727774G>T | CA401039062 | ITGB4 | c.388G>T (p.Val130Leu) n.453G>T n.388G>T c.493G>T (p.Val165Leu) | dbSNP |
| 17 | g.75727775del | CA2639874241 | ITGB4 | c.389del (p.Val130GlyfsTer?) n.454del n.389del c.494del (p.Val165GlyfsTer?) | gnomAD v4 |
| 17 | g.75727775T>A | CA401039063 | ITGB4 | c.389T>A (p.Val130Glu) n.454T>A n.389T>A c.494T>A (p.Val165Glu) | |
| 17 | g.75727775T>C | CA401039064 | ITGB4 | c.389T>C (p.Val130Ala) n.454T>C n.389T>C c.494T>C (p.Val165Ala) | |
| 17 | g.75727775T>G | CA401039065 | ITGB4 | c.389T>G (p.Val130Gly) n.454T>G n.389T>G c.494T>G (p.Val165Gly) | |
| 17 | g.75727776G>A | CA501832196 | ITGB4 | c.390G>A (p.Val130=) n.455G>A n.390G>A c.495G>A (p.Val165=) | |
| 17 | g.75727776G>C | CA501832197 | ITGB4 | c.390G>C (p.Val130=) n.455G>C n.390G>C c.495G>C (p.Val165=) | |
| 17 | g.75727776G>T | CA501832198 | ITGB4 | c.390G>T (p.Val130=) n.455G>T n.390G>T c.495G>T (p.Val165=) | |
| 17 | g.75727777G>A | CA401039068 | ITGB4 | c.391G>A (p.Asp131Asn) n.456G>A n.391G>A c.496G>A (p.Asp166Asn) | |
| 17 | g.75727777G>C | CA401039067 | ITGB4 | c.391G>C (p.Asp131His) n.456G>C n.391G>C c.496G>C (p.Asp166His) | |
| 17 | g.75727777G>T | CA401039066 | ITGB4 | c.391G>T (p.Asp131Tyr) n.456G>T n.391G>T c.496G>T (p.Asp166Tyr) | |
| 17 | g.75727778A= | CA2275653877 | ITGB4 | c.392A= (p.Asp131=) n.457A= n.392A= c.497A= (p.Asp166=) | |
| 17 | g.75727778A>C | CA401039069 | ITGB4 | c.392A>C (p.Asp131Ala) n.457A>C n.392A>C c.497A>C (p.Asp166Ala) | |
| 17 | g.75727778A>G | CA294058670 | ITGB4 | c.392A>G (p.Asp131Gly) n.457A>G n.392A>G c.497A>G (p.Asp166Gly) | dbSNP |
| 17 | g.75727778A>T | CA401039070 | ITGB4 | c.392A>T (p.Asp131Val) n.457A>T n.392A>T c.497A>T (p.Asp166Val) | gnomAD v4 |
| 17 | g.75727779C>A | CA401039071 | ITGB4 | c.393C>A (p.Asp131Glu) n.458C>A n.393C>A c.498C>A (p.Asp166Glu) | |
| 17 | g.75727779C>G | CA401039072 | ITGB4 | c.393C>G (p.Asp131Glu) n.458C>G n.393C>G c.498C>G (p.Asp166Glu) | gnomAD v4 |
| 17 | g.75727779C>T | CA501832199 | ITGB4 | c.393C>T (p.Asp131=) n.458C>T n.393C>T c.498C>T (p.Asp166=) | |
| 17 | g.75727780C>A | CA401039073 | ITGB4 | c.394C>A (p.Leu132Met) n.459C>A n.394C>A c.499C>A (p.Leu167Met) | |
| 17 | g.75727780C= | CA2275653878 | ITGB4 | c.394C= (p.Leu132=) n.459C= n.394C= c.499C= (p.Leu167=) | |
| 17 | g.75727780C>G | CA401039074 | ITGB4 | c.394C>G (p.Leu132Val) n.459C>G n.394C>G c.499C>G (p.Leu167Val) | |
| 17 | g.75727780C>T | CA501832200 | ITGB4 | c.394C>T (p.Leu132=) n.459C>T n.394C>T c.499C>T (p.Leu167=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727781del | CA2695227007 | ITGB4 | c.395del (p.Leu132ArgfsTer29) n.460del n.395del c.500del (p.Leu167ArgfsTer29) | |
| 17 | g.75727781T>A | CA401039075 | ITGB4 | c.395T>A (p.Leu132Gln) n.460T>A n.395T>A c.500T>A (p.Leu167Gln) | |
| 17 | g.75727781T>C | CA401039076 | ITGB4 | c.395T>C (p.Leu132Pro) n.460T>C n.395T>C c.500T>C (p.Leu167Pro) | |
| 17 | g.75727781T>G | CA401039077 | ITGB4 | c.395T>G (p.Leu132Arg) n.460T>G n.395T>G c.500T>G (p.Leu167Arg) | |
| 17 | g.75727782G>A | CA501832201 | ITGB4 | c.396G>A (p.Leu132=) n.461G>A n.396G>A c.501G>A (p.Leu167=) | gnomAD v4 |
| 17 | g.75727782G>C | CA8768656 | ITGB4 | c.396G>C (p.Leu132=) n.461G>C n.396G>C c.501G>C (p.Leu167=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.75727782G= | CA2275653879 | ITGB4 | c.396G= (p.Leu132=) n.461G= n.396G= c.501G= (p.Leu167=) | |
| 17 | g.75727782G>T | CA501832202 | ITGB4 | c.396G>T (p.Leu132=) n.461G>T n.396G>T c.501G>T (p.Leu167=) | |
| 17 | g.75727783T>A | CA401039078 | ITGB4 | c.397T>A (p.Tyr133Asn) n.462T>A n.397T>A c.502T>A (p.Tyr168Asn) | |
| 17 | g.75727783T>C | CA401039079 | ITGB4 | c.397T>C (p.Tyr133His) n.462T>C n.397T>C c.502T>C (p.Tyr168His) | |
| 17 | g.75727783T>G | CA401039080 | ITGB4 | c.397T>G (p.Tyr133Asp) n.462T>G n.397T>G c.502T>G (p.Tyr168Asp) | |
| 17 | g.75727784A>C | CA401039082 | ITGB4 | c.398A>C (p.Tyr133Ser) n.463A>C n.398A>C c.503A>C (p.Tyr168Ser) | |
| 17 | g.75727784A>G | CA401039083 | ITGB4 | c.398A>G (p.Tyr133Cys) n.463A>G n.398A>G c.503A>G (p.Tyr168Cys) | |
| 17 | g.75727784A>T | CA401039081 | ITGB4 | c.398A>T (p.Tyr133Phe) n.463A>T n.398A>T c.503A>T (p.Tyr168Phe) | |
| 17 | g.75727785C>A | CA401039084 | ITGB4 | c.399C>A (p.Tyr133Ter) n.464C>A n.399C>A c.504C>A (p.Tyr168Ter) | |
| 17 | g.75727785C>G | CA401039085 | ITGB4 | c.399C>G (p.Tyr133Ter) n.464C>G n.399C>G c.504C>G (p.Tyr168Ter) | |
| 17 | g.75727785C>T | CA501832203 | ITGB4 | c.399C>T (p.Tyr133=) n.464C>T n.399C>T c.504C>T (p.Tyr168=) | gnomAD v4 |
| 17 | g.75727786A= | CA2275653880 | ITGB4 | c.400A= (p.Ile134=) n.465A= n.400A= c.505A= (p.Ile169=) | |
| 17 | g.75727786A>C | CA8768657 | ITGB4 | c.400A>C (p.Ile134Leu) n.465A>C n.400A>C c.505A>C (p.Ile169Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.75727786A>G | CA401039086 | ITGB4 | c.400A>G (p.Ile134Val) n.465A>G n.400A>G c.505A>G (p.Ile169Val) | |
| 17 | g.75727786A>T | CA401039087 | ITGB4 | c.400A>T (p.Ile134Phe) n.465A>T n.400A>T c.505A>T (p.Ile169Phe) | |
| 17 | g.75727787T>A | CA401039088 | ITGB4 | c.401T>A (p.Ile134Asn) n.466T>A n.401T>A c.506T>A (p.Ile169Asn) | |
| 17 | g.75727787T>C | CA401039089 | ITGB4 | c.401T>C (p.Ile134Thr) n.466T>C n.401T>C c.506T>C (p.Ile169Thr) | |
| 17 | g.75727787T>G | CA401039090 | ITGB4 | c.401T>G (p.Ile134Ser) n.466T>G n.401T>G c.506T>G (p.Ile169Ser) | |
| 17 | g.75727788C>A | CA501832204 | ITGB4 | c.402C>A (p.Ile134=) n.467C>A n.402C>A c.507C>A (p.Ile169=) | |
| 17 | g.75727788C>G | CA401039091 | ITGB4 | c.402C>G (p.Ile134Met) n.467C>G n.402C>G c.507C>G (p.Ile169Met) | |
| 17 | g.75727788C>T | CA501832205 | ITGB4 | c.402C>T (p.Ile134=) n.467C>T n.402C>T c.507C>T (p.Ile169=) | |
| 17 | g.75727789C>A | CA401039092 | ITGB4 | c.403C>A (p.Leu135Ile) n.468C>A n.403C>A c.508C>A (p.Leu170Ile) | |
| 17 | g.75727789C>G | CA401039093 | ITGB4 | c.403C>G (p.Leu135Val) n.468C>G n.403C>G c.508C>G (p.Leu170Val) | |
| 17 | g.75727789C>T | CA401039094 | ITGB4 | c.403C>T (p.Leu135Phe) n.468C>T n.403C>T c.508C>T (p.Leu170Phe) | |
| 17 | g.75727790T>A | CA401039097 | ITGB4 | c.404T>A (p.Leu135His) n.469T>A n.404T>A c.509T>A (p.Leu170His) | |
| 17 | g.75727790T>C | CA401039096 | ITGB4 | c.404T>C (p.Leu135Pro) n.469T>C n.404T>C c.509T>C (p.Leu170Pro) | gnomAD v4 |
| 17 | g.75727790T>G | CA401039095 | ITGB4 | c.404T>G (p.Leu135Arg) n.469T>G n.404T>G c.509T>G (p.Leu170Arg) | |
| 17 | g.75727791C>A | CA501832206 | ITGB4 | c.405C>A (p.Leu135=) n.470C>A n.405C>A c.510C>A (p.Leu170=) | |
| 17 | g.75727791C= | CA2275653881 | ITGB4 | c.405C= (p.Leu135=) n.470C= n.405C= c.510C= (p.Leu170=) | |
| 17 | g.75727791C>G | CA501832208 | ITGB4 | c.405C>G (p.Leu135=) n.470C>G n.405C>G c.510C>G (p.Leu170=) | |
| 17 | g.75727791C>T | CA501832207 | ITGB4 | c.405C>T (p.Leu135=) n.470C>T n.405C>T c.510C>T (p.Leu170=) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.75727792A>C | CA401039098 | ITGB4 | c.406A>C (p.Met136Leu) n.471A>C n.406A>C c.511A>C (p.Met171Leu) | |
| 17 | g.75727792A>G | CA401039099 | ITGB4 | c.406A>G (p.Met136Val) n.471A>G n.406A>G c.511A>G (p.Met171Val) | |
| 17 | g.75727792A>T | CA401039100 | ITGB4 | c.406A>T (p.Met136Leu) n.471A>T n.406A>T c.511A>T (p.Met171Leu) | |
| 17 | g.75727793T>A | CA8768658 | ITGB4 | c.407T>A (p.Met136Lys) n.472T>A n.407T>A c.512T>A (p.Met171Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727793T>C | CA401039101 | ITGB4 | c.407T>C (p.Met136Thr) n.472T>C n.407T>C c.512T>C (p.Met171Thr) | gnomAD v4 |
| 17 | g.75727793T>G | CA401039102 | ITGB4 | c.407T>G (p.Met136Arg) n.472T>G n.407T>G c.512T>G (p.Met171Arg) | |
| 17 | g.75727793T= | CA2275653882 | ITGB4 | c.407T= (p.Met136=) n.472T= n.407T= c.512T= (p.Met171=) | |
| 17 | g.75727794G>A | CA401039103 | ITGB4 | c.408G>A (p.Met136Ile) n.473G>A n.408G>A c.513G>A (p.Met171Ile) | |
| 17 | g.75727794G>C | CA401039104 | ITGB4 | c.408G>C (p.Met136Ile) n.473G>C n.408G>C c.513G>C (p.Met171Ile) | |
| 17 | g.75727794G>T | CA401039105 | ITGB4 | c.408G>T (p.Met136Ile) n.473G>T n.408G>T c.513G>T (p.Met171Ile) | |
| 17 | g.75727795G>A | CA401039106 | ITGB4 | c.409G>A (p.Asp137Asn) n.474G>A n.409G>A c.514G>A (p.Asp172Asn) | |
| 17 | g.75727795G>C | CA401039107 | ITGB4 | c.409G>C (p.Asp137His) n.474G>C n.409G>C c.514G>C (p.Asp172His) | |
| 17 | g.75727795G>T | CA401039108 | ITGB4 | c.409G>T (p.Asp137Tyr) n.474G>T n.409G>T c.514G>T (p.Asp172Tyr) | |
| 17 | g.75727796A>C | CA401039109 | ITGB4 | c.410A>C (p.Asp137Ala) n.475A>C n.410A>C c.515A>C (p.Asp172Ala) | |
| 17 | g.75727796A>G | CA401039111 | ITGB4 | c.410A>G (p.Asp137Gly) n.475A>G n.410A>G c.515A>G (p.Asp172Gly) | |
| 17 | g.75727796A>T | CA401039110 | ITGB4 | c.410A>T (p.Asp137Val) n.475A>T n.410A>T c.515A>T (p.Asp172Val) | |
| 17 | g.75727797C>A | CA401039112 | ITGB4 | c.411C>A (p.Asp137Glu) n.476C>A n.411C>A c.516C>A (p.Asp172Glu) | |
| 17 | g.75727797C= | CA2275653883 | ITGB4 | c.411C= (p.Asp137=) n.476C= n.411C= c.516C= (p.Asp172=) | |
| 17 | g.75727797C>G | CA401039113 | ITGB4 | c.411C>G (p.Asp137Glu) n.476C>G n.411C>G c.516C>G (p.Asp172Glu) | |
| 17 | g.75727797C>T | CA294058672 | ITGB4 | c.411C>T (p.Asp137=) n.476C>T n.411C>T c.516C>T (p.Asp172=) | dbSNP |
| 17 | g.75727798T>A | CA401039114 | ITGB4 | c.412T>A (p.Phe138Ile) n.477T>A n.412T>A c.517T>A (p.Phe173Ile) | |
| 17 | g.75727798T>C | CA401039116 | ITGB4 | c.412T>C (p.Phe138Leu) n.477T>C n.412T>C c.517T>C (p.Phe173Leu) | gnomAD v4 |
| 17 | g.75727798T>G | CA401039115 | ITGB4 | c.412T>G (p.Phe138Val) n.477T>G n.412T>G c.517T>G (p.Phe173Val) | |
| 17 | g.75727799T>A | CA401039117 | ITGB4 | c.413T>A (p.Phe138Tyr) n.478T>A n.413T>A c.518T>A (p.Phe173Tyr) | |
| 17 | g.75727799T>C | CA401039118 | ITGB4 | c.413T>C (p.Phe138Ser) n.478T>C n.413T>C c.518T>C (p.Phe173Ser) | COSMIC COSMIC |
| 17 | g.75727799T>G | CA401039119 | ITGB4 | c.413T>G (p.Phe138Cys) n.478T>G n.413T>G c.518T>G (p.Phe173Cys) | |
| 17 | g.75727800C>A | CA401039120 | ITGB4 | c.414C>A (p.Phe138Leu) n.479C>A n.414C>A c.519C>A (p.Phe173Leu) | |
| 17 | g.75727800C>G | CA401039121 | ITGB4 | c.414C>G (p.Phe138Leu) n.479C>G n.414C>G c.519C>G (p.Phe173Leu) | |
| 17 | g.75727800C>T | CA501832209 | ITGB4 | c.414C>T (p.Phe138=) n.479C>T n.414C>T c.519C>T (p.Phe173=) | COSMIC COSMIC |
| 17 | g.75727801T>A | CA401039124 | ITGB4 | c.415T>A (p.Ser139Thr) n.480T>A c.1T>A (p.Ser1Thr) n.415T>A c.520T>A (p.Ser174Thr) | |
| 17 | g.75727801T>C | CA401039123 | ITGB4 | c.415T>C (p.Ser139Pro) n.480T>C c.1T>C (p.Ser1Pro) n.415T>C c.520T>C (p.Ser174Pro) | gnomAD v4 |
| 17 | g.75727801T>G | CA401039122 | ITGB4 | c.415T>G (p.Ser139Ala) n.480T>G c.1T>G (p.Ser1Ala) n.415T>G c.520T>G (p.Ser174Ala) | |
| 17 | g.75727802C>A | CA401039125 | ITGB4 | c.416C>A (p.Ser139Tyr) n.481C>A c.2C>A (p.Ser1Tyr) n.416C>A c.521C>A (p.Ser174Tyr) | |
| 17 | g.75727802C>G | CA401039126 | ITGB4 | c.416C>G (p.Ser139Cys) n.481C>G c.2C>G (p.Ser1Cys) n.416C>G c.521C>G (p.Ser174Cys) | COSMIC COSMIC |
| 17 | g.75727802C>T | CA401039127 | ITGB4 | c.416C>T (p.Ser139Phe) n.481C>T c.2C>T (p.Ser1Phe) n.416C>T c.521C>T (p.Ser174Phe) | |
| 17 | g.75727803C>A | CA501832210 | ITGB4 | c.417C>A (p.Ser139=) n.482C>A c.3C>A (p.Ser1=) n.417C>A c.522C>A (p.Ser174=) | |
| 17 | g.75727803C= | CA2275653884 | ITGB4 | c.417C= (p.Ser139=) n.482C= c.3C= (p.Ser1=) n.417C= c.522C= (p.Ser174=) | |
| 17 | g.75727803C>G | CA501832211 | ITGB4 | c.417C>G (p.Ser139=) n.482C>G c.3C>G (p.Ser1=) n.417C>G c.522C>G (p.Ser174=) | |
| 17 | g.75727803C>T | CA501832212 | ITGB4 | c.417C>T (p.Ser139=) n.482C>T c.3C>T (p.Ser1=) n.417C>T c.522C>T (p.Ser174=) | dbSNP gnomAD v4 |
| 17 | g.75727804A>C | CA401039128 | ITGB4 | c.418A>C (p.Asn140His) n.483A>C c.4A>C (p.Asn2His) n.418A>C c.523A>C (p.Asn175His) | |
| 17 | g.75727804A>G | CA401039129 | ITGB4 | c.418A>G (p.Asn140Asp) n.483A>G c.4A>G (p.Asn2Asp) n.418A>G c.523A>G (p.Asn175Asp) | |
| 17 | g.75727804A>T | CA401039130 | ITGB4 | c.418A>T (p.Asn140Tyr) n.483A>T c.4A>T (p.Asn2Tyr) n.418A>T c.523A>T (p.Asn175Tyr) | |
| 17 | g.75727805A>C | CA401039131 | ITGB4 | c.419A>C (p.Asn140Thr) n.484A>C c.5A>C (p.Asn2Thr) n.419A>C c.524A>C (p.Asn175Thr) | |
| 17 | g.75727805A>G | CA401039133 | ITGB4 | c.419A>G (p.Asn140Ser) n.484A>G c.5A>G (p.Asn2Ser) n.419A>G c.524A>G (p.Asn175Ser) | |
| 17 | g.75727805A>T | CA401039132 | ITGB4 | c.419A>T (p.Asn140Ile) n.484A>T c.5A>T (p.Asn2Ile) n.419A>T c.524A>T (p.Asn175Ile) | |
| 17 | g.75727806C>A | CA401039134 | ITGB4 | c.420C>A (p.Asn140Lys) n.485C>A c.6C>A (p.Asn2Lys) n.420C>A c.525C>A (p.Asn175Lys) | |
| 17 | g.75727806C>G | CA401039135 | ITGB4 | c.420C>G (p.Asn140Lys) n.485C>G c.6C>G (p.Asn2Lys) n.420C>G c.525C>G (p.Asn175Lys) | |
| 17 | g.75727806C>T | CA501832213 | ITGB4 | c.420C>T (p.Asn140=) n.485C>T c.6C>T (p.Asn2=) n.420C>T c.525C>T (p.Asn175=) | |
| 17 | g.75727807T>A | CA401039136 | ITGB4 | c.421T>A (p.Ser141Thr) n.486T>A c.7T>A (p.Ser3Thr) n.421T>A c.526T>A (p.Ser176Thr) | |
| 17 | g.75727807T>C | CA401039137 | ITGB4 | c.421T>C (p.Ser141Pro) n.486T>C c.7T>C (p.Ser3Pro) n.421T>C c.526T>C (p.Ser176Pro) | |
| 17 | g.75727807T>G | CA401039138 | ITGB4 | c.421T>G (p.Ser141Ala) n.486T>G c.7T>G (p.Ser3Ala) n.421T>G c.526T>G (p.Ser176Ala) | |
| 17 | g.75727807_75727808delinsTC | CA2275653885 | ITGB4 | c.421_422delinsTC (p.Ser141=) n.486_487delinsTC c.7_8delinsTC (p.Ser3=) n.421_422delinsTC c.526_527delinsTC (p.Ser176=) | |
| 17 | g.75727808C>A | CA401039139 | ITGB4 | c.422C>A (p.Ser141Tyr) n.487C>A c.8C>A (p.Ser3Tyr) n.422C>A c.527C>A (p.Ser176Tyr) | |
| 17 | g.75727808C>G | CA401039140 | ITGB4 | c.422C>G (p.Ser141Cys) n.487C>G c.8C>G (p.Ser3Cys) n.422C>G c.527C>G (p.Ser176Cys) | |
| 17 | g.75727808C>T | CA401039141 | ITGB4 | c.422C>T (p.Ser141Phe) n.487C>T c.8C>T (p.Ser3Phe) n.422C>T c.527C>T (p.Ser176Phe) | COSMIC COSMIC |
| 17 | g.75727809del | CA775096730 | ITGB4 | c.423del (p.Met142CysfsTer19) n.488del c.9del (p.Met4CysfsTer19) n.423del c.528del (p.Met177CysfsTer19) | dbSNP |
| 17 | g.75727809C>A | CA501832214 | ITGB4 | c.423C>A (p.Ser141=) n.488C>A c.9C>A (p.Ser3=) n.423C>A c.528C>A (p.Ser176=) | |
| 17 | g.75727809C= | CA2275653886 | ITGB4 | c.423C= (p.Ser141=) n.488C= c.9C= (p.Ser3=) n.423C= c.528C= (p.Ser176=) | |
| 17 | g.75727809C>G | CA501832215 | ITGB4 | c.423C>G (p.Ser141=) n.488C>G c.9C>G (p.Ser3=) n.423C>G c.528C>G (p.Ser176=) | |
| 17 | g.75727809C>T | CA501832216 | ITGB4 | c.423C>T (p.Ser141=) n.488C>T c.9C>T (p.Ser3=) n.423C>T c.528C>T (p.Ser176=) | dbSNP |
| 17 | g.75727810A= | CA2275653887 | ITGB4 | c.424A= (p.Met142=) n.489A= c.10A= (p.Met4=) n.424A= c.529A= (p.Met177=) | |
| 17 | g.75727810A>C | CA401039142 | ITGB4 | c.424A>C (p.Met142Leu) n.489A>C c.10A>C (p.Met4Leu) n.424A>C c.529A>C (p.Met177Leu) | |
| 17 | g.75727810A>G | CA401039143 | ITGB4 | c.424A>G (p.Met142Val) n.489A>G c.10A>G (p.Met4Val) n.424A>G c.529A>G (p.Met177Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727810A>T | CA401039144 | ITGB4 | c.424A>T (p.Met142Leu) n.489A>T c.10A>T (p.Met4Leu) n.424A>T c.529A>T (p.Met177Leu) | |
| 17 | g.75727811T>A | CA401039145 | ITGB4 | c.425T>A (p.Met142Lys) n.490T>A c.11T>A (p.Met4Lys) n.425T>A c.530T>A (p.Met177Lys) | |
| 17 | g.75727811T>C | CA401039147 | ITGB4 | c.425T>C (p.Met142Thr) n.490T>C c.11T>C (p.Met4Thr) n.425T>C c.530T>C (p.Met177Thr) | gnomAD v4 |
| 17 | g.75727811T>G | CA401039146 | ITGB4 | c.425T>G (p.Met142Arg) n.490T>G c.11T>G (p.Met4Arg) n.425T>G c.530T>G (p.Met177Arg) | |
| 17 | g.75727812G>A | CA401039148 | ITGB4 | c.426G>A (p.Met142Ile) n.491G>A c.12G>A (p.Met4Ile) n.426G>A c.531G>A (p.Met177Ile) | |
| 17 | g.75727812G>C | CA401039149 | ITGB4 | c.426G>C (p.Met142Ile) n.491G>C c.12G>C (p.Met4Ile) n.426G>C c.531G>C (p.Met177Ile) | dbSNP gnomAD v2 gnomAD v4 |
| 17 | g.75727812G= | CA2275653888 | ITGB4 | c.426G= (p.Met142=) n.491G= c.12G= (p.Met4=) n.426G= c.531G= (p.Met177=) | |
| 17 | g.75727812G>T | CA401039150 | ITGB4 | c.426G>T (p.Met142Ile) n.491G>T c.12G>T (p.Met4Ile) n.426G>T c.531G>T (p.Met177Ile) | |
| 17 | g.75727813T>A | CA401039151 | ITGB4 | c.427T>A (p.Ser143Thr) n.492T>A c.13T>A (p.Ser5Thr) n.427T>A c.532T>A (p.Ser178Thr) | |
| 17 | g.75727813T>C | CA401039152 | ITGB4 | c.427T>C (p.Ser143Pro) n.492T>C c.13T>C (p.Ser5Pro) n.427T>C c.532T>C (p.Ser178Pro) | |
| 17 | g.75727813T>G | CA401039153 | ITGB4 | c.427T>G (p.Ser143Ala) n.492T>G c.13T>G (p.Ser5Ala) n.427T>G c.532T>G (p.Ser178Ala) | |
| 17 | g.75727814C>A | CA401039154 | ITGB4 | c.428C>A (p.Ser143Tyr) n.493C>A c.14C>A (p.Ser5Tyr) n.428C>A c.533C>A (p.Ser178Tyr) | gnomAD v4 |
| 17 | g.75727814C>G | CA401039155 | ITGB4 | c.428C>G (p.Ser143Cys) n.493C>G c.14C>G (p.Ser5Cys) n.428C>G c.533C>G (p.Ser178Cys) | |
| 17 | g.75727814C>T | CA401039156 | ITGB4 | c.428C>T (p.Ser143Phe) n.493C>T c.14C>T (p.Ser5Phe) n.428C>T c.533C>T (p.Ser178Phe) | |
| 17 | g.75727815C>A | CA501832217 | ITGB4 | c.429C>A (p.Ser143=) n.494C>A c.15C>A (p.Ser5=) n.429C>A c.534C>A (p.Ser178=) | |
| 17 | g.75727815C= | CA2275653889 | ITGB4 | c.429C= (p.Ser143=) n.494C= c.15C= (p.Ser5=) n.429C= c.534C= (p.Ser178=) | |
| 17 | g.75727815C>G | CA501832218 | ITGB4 | c.429C>G (p.Ser143=) n.494C>G c.15C>G (p.Ser5=) n.429C>G c.534C>G (p.Ser178=) | |
| 17 | g.75727815C>T | CA501832219 | ITGB4 | c.429C>T (p.Ser143=) n.494C>T c.15C>T (p.Ser5=) n.429C>T c.534C>T (p.Ser178=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727816G>A | CA401039157 | ITGB4 | c.430G>A (p.Asp144Asn) n.495G>A c.16G>A (p.Asp6Asn) n.430G>A c.535G>A (p.Asp179Asn) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727816G>C | CA401039158 | ITGB4 | c.430G>C (p.Asp144His) n.495G>C c.16G>C (p.Asp6His) n.430G>C c.535G>C (p.Asp179His) | |
| 17 | g.75727816G= | CA2275653890 | ITGB4 | c.430G= (p.Asp144=) n.495G= c.16G= (p.Asp6=) n.430G= c.535G= (p.Asp179=) | |
| 17 | g.75727816G>T | CA401039159 | ITGB4 | c.430G>T (p.Asp144Tyr) n.495G>T c.16G>T (p.Asp6Tyr) n.430G>T c.535G>T (p.Asp179Tyr) | dbSNP |
| 17 | g.75727817A= | CA2275653891 | ITGB4 | c.431A= (p.Asp144=) n.496A= c.17A= (p.Asp6=) n.431A= c.536A= (p.Asp179=) | |
| 17 | g.75727817A>C | CA401039162 | ITGB4 | c.431A>C (p.Asp144Ala) n.496A>C c.17A>C (p.Asp6Ala) n.431A>C c.536A>C (p.Asp179Ala) | |
| 17 | g.75727817A>G | CA401039160 | ITGB4 | c.431A>G (p.Asp144Gly) n.496A>G c.17A>G (p.Asp6Gly) n.431A>G c.536A>G (p.Asp179Gly) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.75727817A>T | CA401039161 | ITGB4 | c.431A>T (p.Asp144Val) n.496A>T c.17A>T (p.Asp6Val) n.431A>T c.536A>T (p.Asp179Val) | |
| 17 | g.75727818T>A | CA401039163 | ITGB4 | c.432T>A (p.Asp144Glu) n.497T>A c.18T>A (p.Asp6Glu) n.432T>A c.537T>A (p.Asp179Glu) | |
| 17 | g.75727818T>C | CA8768659 | ITGB4 | c.432T>C (p.Asp144=) n.497T>C c.18T>C (p.Asp6=) n.432T>C c.537T>C (p.Asp179=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.75727818T>G | CA401039164 | ITGB4 | c.432T>G (p.Asp144Glu) n.497T>G c.18T>G (p.Asp6Glu) n.432T>G c.537T>G (p.Asp179Glu) | gnomAD v4 |
| 17 | g.75727818T= | CA2275653892 | ITGB4 | c.432T= (p.Asp144=) n.497T= c.18T= (p.Asp6=) n.432T= c.537T= (p.Asp179=) | |
| 17 | g.75727819G>A | CA401039165 | ITGB4 | c.433G>A (p.Asp145Asn) n.498G>A c.19G>A (p.Asp7Asn) n.433G>A c.538G>A (p.Asp180Asn) | |
| 17 | g.75727819G>C | CA401039166 | ITGB4 | c.433G>C (p.Asp145His) n.498G>C c.19G>C (p.Asp7His) n.433G>C c.538G>C (p.Asp180His) | |
| 17 | g.75727819G>T | CA401039167 | ITGB4 | c.433G>T (p.Asp145Tyr) n.498G>T c.19G>T (p.Asp7Tyr) n.433G>T c.538G>T (p.Asp180Tyr) | |
| 17 | g.75727820A>C | CA401039168 | ITGB4 | c.434A>C (p.Asp145Ala) n.499A>C c.20A>C (p.Asp7Ala) n.434A>C c.539A>C (p.Asp180Ala) | |
| 17 | g.75727820A>G | CA401039169 | ITGB4 | c.434A>G (p.Asp145Gly) n.499A>G c.20A>G (p.Asp7Gly) n.434A>G c.539A>G (p.Asp180Gly) | |
| 17 | g.75727820A>T | CA401039170 | ITGB4 | c.434A>T (p.Asp145Val) n.499A>T c.20A>T (p.Asp7Val) n.434A>T c.539A>T (p.Asp180Val) | |
| 17 | g.75727821T>A | CA401039171 | ITGB4 | c.435T>A (p.Asp145Glu) n.500T>A c.21T>A (p.Asp7Glu) n.435T>A c.540T>A (p.Asp180Glu) | |
| 17 | g.75727821T>C | CA501832220 | ITGB4 | c.435T>C (p.Asp145=) n.500T>C c.21T>C (p.Asp7=) n.435T>C c.540T>C (p.Asp180=) | ClinVar gnomAD v4 |
| 17 | g.75727821T>G | CA401039172 | ITGB4 | c.435T>G (p.Asp145Glu) n.500T>G c.21T>G (p.Asp7Glu) n.435T>G c.540T>G (p.Asp180Glu) | |
| 17 | g.75727822C>A | CA401039173 | ITGB4 | c.436C>A (p.Leu146Met) n.501C>A c.22C>A (p.Leu8Met) n.436C>A c.541C>A (p.Leu181Met) | |
| 17 | g.75727822C>G | CA401039174 | ITGB4 | c.436C>G (p.Leu146Val) n.501C>G c.22C>G (p.Leu8Val) n.436C>G c.541C>G (p.Leu181Val) | |
| 17 | g.75727822C>T | CA501832221 | ITGB4 | c.436C>T (p.Leu146=) n.501C>T c.22C>T (p.Leu8=) n.436C>T c.541C>T (p.Leu181=) | |
| 17 | g.75727823T>A | CA401039175 | ITGB4 | c.437T>A (p.Leu146Gln) n.502T>A c.23T>A (p.Leu8Gln) n.437T>A c.542T>A (p.Leu181Gln) | |
| 17 | g.75727823T>C | CA401039177 | ITGB4 | c.437T>C (p.Leu146Pro) n.502T>C c.23T>C (p.Leu8Pro) n.437T>C c.542T>C (p.Leu181Pro) | |
| 17 | g.75727823T>G | CA401039176 | ITGB4 | c.437T>G (p.Leu146Arg) n.502T>G c.23T>G (p.Leu8Arg) n.437T>G c.542T>G (p.Leu181Arg) | |
| 17 | g.75727824G>A | CA501832222 | ITGB4 | c.438G>A (p.Leu146=) n.503G>A c.24G>A (p.Leu8=) n.438G>A c.543G>A (p.Leu181=) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.75727824G>C | CA501832223 | ITGB4 | c.438G>C (p.Leu146=) n.503G>C c.24G>C (p.Leu8=) n.438G>C c.543G>C (p.Leu181=) | |
| 17 | g.75727824G= | CA2275653893 | ITGB4 | c.438G= (p.Leu146=) n.503G= c.24G= (p.Leu8=) n.438G= c.543G= (p.Leu181=) | |
| 17 | g.75727824G>T | CA501832224 | ITGB4 | c.438G>T (p.Leu146=) n.503G>T c.24G>T (p.Leu8=) n.438G>T c.543G>T (p.Leu181=) | |
| 17 | g.75727825G>A | CA401039178 | ITGB4 | c.439G>A (p.Asp147Asn) n.504G>A c.25G>A (p.Asp9Asn) n.439G>A c.544G>A (p.Asp182Asn) | |
| 17 | g.75727825G>C | CA401039179 | ITGB4 | c.439G>C (p.Asp147His) n.504G>C c.25G>C (p.Asp9His) n.439G>C c.544G>C (p.Asp182His) | |
| 17 | g.75727825G>T | CA401039180 | ITGB4 | c.439G>T (p.Asp147Tyr) n.504G>T c.25G>T (p.Asp9Tyr) n.439G>T c.544G>T (p.Asp182Tyr) | |
| 17 | g.75727826A>C | CA401039181 | ITGB4 | c.440A>C (p.Asp147Ala) n.505A>C c.26A>C (p.Asp9Ala) n.440A>C c.545A>C (p.Asp182Ala) | |
| 17 | g.75727826A>G | CA401039182 | ITGB4 | c.440A>G (p.Asp147Gly) n.505A>G c.26A>G (p.Asp9Gly) n.440A>G c.545A>G (p.Asp182Gly) | |
| 17 | g.75727826A>T | CA401039183 | ITGB4 | c.440A>T (p.Asp147Val) n.505A>T c.26A>T (p.Asp9Val) n.440A>T c.545A>T (p.Asp182Val) | |
| 17 | g.75727827C>A | CA401039184 | ITGB4 | c.441C>A (p.Asp147Glu) n.506C>A c.27C>A (p.Asp9Glu) n.441C>A c.546C>A (p.Asp182Glu) | |
| 17 | g.75727827C>G | CA401039185 | ITGB4 | c.441C>G (p.Asp147Glu) n.506C>G c.27C>G (p.Asp9Glu) n.441C>G c.546C>G (p.Asp182Glu) | |
| 17 | g.75727827C>T | CA501832225 | ITGB4 | c.441C>T (p.Asp147=) n.506C>T c.27C>T (p.Asp9=) n.441C>T c.546C>T (p.Asp182=) | |
| 17 | g.75727828A>C | CA401039186 | ITGB4 | c.442A>C (p.Asn148His) n.507A>C c.28A>C (p.Asn10His) n.442A>C c.547A>C (p.Asn183His) | |
| 17 | g.75727828A>G | CA401039187 | ITGB4 | c.442A>G (p.Asn148Asp) n.507A>G c.28A>G (p.Asn10Asp) n.442A>G c.547A>G (p.Asn183Asp) | |
| 17 | g.75727828A>T | CA401039188 | ITGB4 | c.442A>T (p.Asn148Tyr) n.507A>T c.28A>T (p.Asn10Tyr) n.442A>T c.547A>T (p.Asn183Tyr) | |
| 17 | g.75727829A>C | CA401039191 | ITGB4 | c.443A>C (p.Asn148Thr) n.508A>C c.29A>C (p.Asn10Thr) n.443A>C c.548A>C (p.Asn183Thr) | |
| 17 | g.75727829A>G | CA401039190 | ITGB4 | c.443A>G (p.Asn148Ser) n.508A>G c.29A>G (p.Asn10Ser) n.443A>G c.548A>G (p.Asn183Ser) | |
| 17 | g.75727829A>T | CA401039189 | ITGB4 | c.443A>T (p.Asn148Ile) n.508A>T c.29A>T (p.Asn10Ile) n.443A>T c.548A>T (p.Asn183Ile) | |
| 17 | g.75727830C>A | CA401039192 | ITGB4 | c.444C>A (p.Asn148Lys) n.509C>A c.30C>A (p.Asn10Lys) n.444C>A c.549C>A (p.Asn183Lys) | |
| 17 | g.75727830C>G | CA401039193 | ITGB4 | c.444C>G (p.Asn148Lys) n.509C>G c.30C>G (p.Asn10Lys) n.444C>G c.549C>G (p.Asn183Lys) | |
| 17 | g.75727830C>T | CA501832226 | ITGB4 | c.444C>T (p.Asn148=) n.509C>T c.30C>T (p.Asn10=) n.444C>T c.549C>T (p.Asn183=) | ClinVar |
| 17 | g.75727831C>A | CA401039194 | ITGB4 | c.445C>A (p.Leu149Ile) n.510C>A c.31C>A (p.Leu11Ile) n.445C>A c.550C>A (p.Leu184Ile) | |
| 17 | g.75727831C= | CA2275653894 | ITGB4 | c.445C= (p.Leu149=) n.510C= c.31C= (p.Leu11=) n.445C= c.550C= (p.Leu184=) | |
| 17 | g.75727831C>G | CA8768660 | ITGB4 | c.445C>G (p.Leu149Val) n.510C>G c.31C>G (p.Leu11Val) n.445C>G c.550C>G (p.Leu184Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727831C>T | CA8768661 | ITGB4 | c.445C>T (p.Leu149Phe) n.510C>T c.31C>T (p.Leu11Phe) n.445C>T c.550C>T (p.Leu184Phe) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727832T>A | CA401039195 | ITGB4 | c.446T>A (p.Leu149His) n.511T>A c.32T>A (p.Leu11His) n.446T>A c.551T>A (p.Leu184His) | |
| 17 | g.75727832T>C | CA401039196 | ITGB4 | c.446T>C (p.Leu149Pro) n.511T>C c.32T>C (p.Leu11Pro) n.446T>C c.551T>C (p.Leu184Pro) | |
| 17 | g.75727832T>G | CA401039197 | ITGB4 | c.446T>G (p.Leu149Arg) n.511T>G c.32T>G (p.Leu11Arg) n.446T>G c.551T>G (p.Leu184Arg) | |
| 17 | g.75727833C>A | CA501832227 | ITGB4 | c.447C>A (p.Leu149=) n.512C>A c.33C>A (p.Leu11=) n.447C>A c.552C>A (p.Leu184=) | |
| 17 | g.75727833C>G | CA501832229 | ITGB4 | c.447C>G (p.Leu149=) n.512C>G c.33C>G (p.Leu11=) n.447C>G c.552C>G (p.Leu184=) | |
| 17 | g.75727833C>T | CA501832228 | ITGB4 | c.447C>T (p.Leu149=) n.512C>T c.33C>T (p.Leu11=) n.447C>T c.552C>T (p.Leu184=) | |
| 17 | g.75727834A>C | CA401039198 | ITGB4 | c.448A>C (p.Lys150Gln) n.513A>C c.34A>C (p.Lys12Gln) n.448A>C c.553A>C (p.Lys185Gln) | gnomAD v4 |
| 17 | g.75727834A>G | CA401039199 | ITGB4 | c.448A>G (p.Lys150Glu) n.513A>G c.34A>G (p.Lys12Glu) n.448A>G c.553A>G (p.Lys185Glu) | |
| 17 | g.75727834A>T | CA401039200 | ITGB4 | c.448A>T (p.Lys150Ter) n.513A>T c.34A>T (p.Lys12Ter) n.448A>T c.553A>T (p.Lys185Ter) | |
| 17 | g.75727835A= | CA2275653895 | ITGB4 | c.449A= (p.Lys150=) n.514A= c.35A= (p.Lys12=) n.449A= c.554A= (p.Lys185=) | |
| 17 | g.75727835A>C | CA401039203 | ITGB4 | c.449A>C (p.Lys150Thr) n.514A>C c.35A>C (p.Lys12Thr) n.449A>C c.554A>C (p.Lys185Thr) | |
| 17 | g.75727835A>G | CA401039202 | ITGB4 | c.449A>G (p.Lys150Arg) n.514A>G c.35A>G (p.Lys12Arg) n.449A>G c.554A>G (p.Lys185Arg) | dbSNP gnomAD v4 |
| 17 | g.75727835A>T | CA401039201 | ITGB4 | c.449A>T (p.Lys150Met) n.514A>T c.35A>T (p.Lys12Met) n.449A>T c.554A>T (p.Lys185Met) | |
| 17 | g.75727836G>A | CA501832230 | ITGB4 | c.450G>A (p.Lys150=) n.515G>A c.36G>A (p.Lys12=) n.450G>A c.555G>A (p.Lys185=) | |
| 17 | g.75727836G>C | CA401039204 | ITGB4 | c.450G>C (p.Lys150Asn) n.515G>C c.36G>C (p.Lys12Asn) n.450G>C c.555G>C (p.Lys185Asn) | |
| 17 | g.75727836G>T | CA401039205 | ITGB4 | c.450G>T (p.Lys150Asn) n.515G>T c.36G>T (p.Lys12Asn) n.450G>T c.555G>T (p.Lys185Asn) | |
| 17 | g.75727837A= | CA2275653896 | ITGB4 | c.451A= (p.Lys151=) n.516A= c.37A= (p.Lys13=) n.451A= c.556A= (p.Lys186=) | |
| 17 | g.75727837A>C | CA401039206 | ITGB4 | c.451A>C (p.Lys151Gln) n.516A>C c.37A>C (p.Lys13Gln) n.451A>C c.556A>C (p.Lys186Gln) | |
| 17 | g.75727837A>G | CA401039207 | ITGB4 | c.451A>G (p.Lys151Glu) n.516A>G c.37A>G (p.Lys13Glu) n.451A>G c.556A>G (p.Lys186Glu) | dbSNP |
| 17 | g.75727837A>T | CA401039208 | ITGB4 | c.451A>T (p.Lys151Ter) n.516A>T c.37A>T (p.Lys13Ter) n.451A>T c.556A>T (p.Lys186Ter) | |
| 17 | g.75727838A>C | CA401039209 | ITGB4 | c.452A>C (p.Lys151Thr) n.517A>C c.38A>C (p.Lys13Thr) n.452A>C c.557A>C (p.Lys186Thr) | |
| 17 | g.75727838A>G | CA401039210 | ITGB4 | c.452A>G (p.Lys151Arg) n.517A>G c.38A>G (p.Lys13Arg) n.452A>G c.557A>G (p.Lys186Arg) | |
| 17 | g.75727838A>T | CA401039211 | ITGB4 | c.452A>T (p.Lys151Met) n.517A>T c.38A>T (p.Lys13Met) n.452A>T c.557A>T (p.Lys186Met) | |
| 17 | g.75727839G>A | CA501832231 | ITGB4 | c.453G>A (p.Lys151=) n.518G>A c.39G>A (p.Lys13=) n.453G>A c.558G>A (p.Lys186=) | |
| 17 | g.75727839G>C | CA401039212 | ITGB4 | c.453G>C (p.Lys151Asn) n.518G>C c.39G>C (p.Lys13Asn) n.453G>C c.558G>C (p.Lys186Asn) | |
| 17 | g.75727839G>T | CA401039213 | ITGB4 | c.453G>T (p.Lys151Asn) n.518G>T c.39G>T (p.Lys13Asn) n.453G>T c.558G>T (p.Lys186Asn) | |
| 17 | g.75727840A>C | CA401039214 | ITGB4 | c.454A>C (p.Met152Leu) n.519A>C c.40A>C (p.Met14Leu) n.454A>C c.559A>C (p.Met187Leu) | |
| 17 | g.75727840A>G | CA401039215 | ITGB4 | c.454A>G (p.Met152Val) n.519A>G c.40A>G (p.Met14Val) n.454A>G c.559A>G (p.Met187Val) | |
| 17 | g.75727840A>T | CA401039216 | ITGB4 | c.454A>T (p.Met152Leu) n.519A>T c.40A>T (p.Met14Leu) n.454A>T c.559A>T (p.Met187Leu) | |
| 17 | g.75727841T>A | CA401039219 | ITGB4 | c.455T>A (p.Met152Lys) n.520T>A c.41T>A (p.Met14Lys) n.455T>A c.560T>A (p.Met187Lys) | |
| 17 | g.75727841T>C | CA401039217 | ITGB4 | c.455T>C (p.Met152Thr) n.520T>C c.41T>C (p.Met14Thr) n.455T>C c.560T>C (p.Met187Thr) | |
| 17 | g.75727841T>G | CA401039218 | ITGB4 | c.455T>G (p.Met152Arg) n.520T>G c.41T>G (p.Met14Arg) n.455T>G c.560T>G (p.Met187Arg) | |
| 17 | g.75727842G>A | CA8768662 | ITGB4 | c.456G>A (p.Met152Ile) n.521G>A c.42G>A (p.Met14Ile) n.456G>A c.561G>A (p.Met187Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727842G>C | CA401039220 | ITGB4 | c.456G>C (p.Met152Ile) n.521G>C c.42G>C (p.Met14Ile) n.456G>C c.561G>C (p.Met187Ile) | |
| 17 | g.75727842G= | CA2275653897 | ITGB4 | c.456G= (p.Met152=) n.521G= c.42G= (p.Met14=) n.456G= c.561G= (p.Met187=) | |
| 17 | g.75727842G>T | CA401039221 | ITGB4 | c.456G>T (p.Met152Ile) n.521G>T c.42G>T (p.Met14Ile) n.456G>T c.561G>T (p.Met187Ile) | |
| 17 | g.75727843G>A | CA401039222 | ITGB4 | c.457G>A (p.Gly153Arg) n.522G>A c.43G>A (p.Gly15Arg) n.457G>A c.562G>A (p.Gly188Arg) | gnomAD v4 |
| 17 | g.75727843G>C | CA401039223 | ITGB4 | c.457G>C (p.Gly153Arg) n.522G>C c.43G>C (p.Gly15Arg) n.457G>C c.562G>C (p.Gly188Arg) | |
| 17 | g.75727843G>T | CA401039224 | ITGB4 | c.457G>T (p.Gly153Trp) n.522G>T c.43G>T (p.Gly15Trp) n.457G>T c.562G>T (p.Gly188Trp) | |
| 17 | g.75727844G>A | CA401039225 | ITGB4 | c.458G>A (p.Gly153Glu) n.523G>A c.44G>A (p.Gly15Glu) n.458G>A c.563G>A (p.Gly188Glu) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.75727844G>C | CA401039226 | ITGB4 | c.458G>C (p.Gly153Ala) n.523G>C c.44G>C (p.Gly15Ala) n.458G>C c.563G>C (p.Gly188Ala) | |
| 17 | g.75727844G= | CA2275653898 | ITGB4 | c.458G= (p.Gly153=) n.523G= c.44G= (p.Gly15=) n.458G= c.563G= (p.Gly188=) | |
| 17 | g.75727844G>T | CA401039227 | ITGB4 | c.458G>T (p.Gly153Val) n.523G>T c.44G>T (p.Gly15Val) n.458G>T c.563G>T (p.Gly188Val) | |
| 17 | g.75727845G>A | CA501832232 | ITGB4 | c.459G>A (p.Gly153=) n.524G>A c.45G>A (p.Gly15=) n.459G>A c.564G>A (p.Gly188=) | gnomAD v4 |
| 17 | g.75727845G>C | CA501832233 | ITGB4 | c.459G>C (p.Gly153=) n.524G>C c.45G>C (p.Gly15=) n.459G>C c.564G>C (p.Gly188=) | |
| 17 | g.75727845G>T | CA501832234 | ITGB4 | c.459G>T (p.Gly153=) n.524G>T c.45G>T (p.Gly15=) n.459G>T c.564G>T (p.Gly188=) | |
| 17 | g.75727846C>A | CA401039228 | ITGB4 | c.460C>A (p.Gln154Lys) n.525C>A c.46C>A (p.Gln16Lys) n.460C>A c.565C>A (p.Gln189Lys) | |
| 17 | g.75727846C>G | CA401039229 | ITGB4 | c.460C>G (p.Gln154Glu) n.525C>G c.46C>G (p.Gln16Glu) n.460C>G c.565C>G (p.Gln189Glu) | |
| 17 | g.75727846C>T | CA401039230 | ITGB4 | c.460C>T (p.Gln154Ter) n.525C>T c.46C>T (p.Gln16Ter) n.460C>T c.565C>T (p.Gln189Ter) | gnomAD v4 |
| 17 | g.75727847A>C | CA401039232 | ITGB4 | c.461A>C (p.Gln154Pro) n.526A>C c.47A>C (p.Gln16Pro) n.461A>C c.566A>C (p.Gln189Pro) | |
| 17 | g.75727847A>G | CA401039233 | ITGB4 | c.461A>G (p.Gln154Arg) n.526A>G c.47A>G (p.Gln16Arg) n.461A>G c.566A>G (p.Gln189Arg) | |
| 17 | g.75727847A>T | CA401039231 | ITGB4 | c.461A>T (p.Gln154Leu) n.526A>T c.47A>T (p.Gln16Leu) n.461A>T c.566A>T (p.Gln189Leu) | |
| 17 | g.75727848G>A | CA501832235 | ITGB4 | c.462G>A (p.Gln154=) n.527G>A c.48G>A (p.Gln16=) n.462G>A c.567G>A (p.Gln189=) | |
| 17 | g.75727848G>C | CA401039235 | ITGB4 | c.462G>C (p.Gln154His) n.527G>C c.48G>C (p.Gln16His) n.462G>C c.567G>C (p.Gln189His) | |
| 17 | g.75727848G>T | CA401039234 | ITGB4 | c.462G>T (p.Gln154His) n.527G>T c.48G>T (p.Gln16His) n.462G>T c.567G>T (p.Gln189His) | |
| 17 | g.75727849A>C | CA401039238 | ITGB4 | c.463A>C (p.Asn155His) n.528A>C c.49A>C (p.Asn17His) n.463A>C c.568A>C (p.Asn190His) | |
| 17 | g.75727849A>G | CA401039236 | ITGB4 | c.463A>G (p.Asn155Asp) n.528A>G c.49A>G (p.Asn17Asp) n.463A>G c.568A>G (p.Asn190Asp) | |
| 17 | g.75727849A>T | CA401039237 | ITGB4 | c.463A>T (p.Asn155Tyr) n.528A>T c.49A>T (p.Asn17Tyr) n.463A>T c.568A>T (p.Asn190Tyr) | |
| 17 | g.75727850A>C | CA401039239 | ITGB4 | c.464A>C (p.Asn155Thr) n.529A>C c.50A>C (p.Asn17Thr) n.464A>C c.569A>C (p.Asn190Thr) | |
| 17 | g.75727850A>G | CA401039240 | ITGB4 | c.464A>G (p.Asn155Ser) n.529A>G c.50A>G (p.Asn17Ser) n.464A>G c.569A>G (p.Asn190Ser) | |
| 17 | g.75727850A>T | CA401039241 | ITGB4 | c.464A>T (p.Asn155Ile) n.529A>T c.50A>T (p.Asn17Ile) n.464A>T c.569A>T (p.Asn190Ile) | |
| 17 | g.75727851C>A | CA401039242 | ITGB4 | c.465C>A (p.Asn155Lys) n.530C>A c.51C>A (p.Asn17Lys) n.465C>A c.570C>A (p.Asn190Lys) | |
| 17 | g.75727851C= | CA2275653899 | ITGB4 | c.465C= (p.Asn155=) n.530C= c.51C= (p.Asn17=) n.465C= c.570C= (p.Asn190=) | |
| 17 | g.75727851C>G | CA401039244 | ITGB4 | c.465C>G (p.Asn155Lys) n.530C>G c.51C>G (p.Asn17Lys) n.465C>G c.570C>G (p.Asn190Lys) | dbSNP gnomAD v3 gnomAD v4 |
| 17 | g.75727851C>T | CA501832236 | ITGB4 | c.465C>T (p.Asn155=) n.530C>T c.51C>T (p.Asn17=) n.465C>T c.570C>T (p.Asn190=) | |
| 17 | g.75727852C>A | CA401039246 | ITGB4 | c.466C>A (p.Leu156Met) n.531C>A c.52C>A (p.Leu18Met) n.466C>A c.571C>A (p.Leu191Met) | |
| 17 | g.75727852C>G | CA401039248 | ITGB4 | c.466C>G (p.Leu156Val) n.531C>G c.52C>G (p.Leu18Val) n.466C>G c.571C>G (p.Leu191Val) | |
| 17 | g.75727852C>T | CA501832237 | ITGB4 | c.466C>T (p.Leu156=) n.531C>T c.52C>T (p.Leu18=) n.466C>T c.571C>T (p.Leu191=) | |
| 17 | g.75727853T>A | CA401039252 | ITGB4 | c.467T>A (p.Leu156Gln) n.532T>A c.53T>A (p.Leu18Gln) n.467T>A c.572T>A (p.Leu191Gln) | |
| 17 | g.75727853T>C | CA257298 | ITGB4 | c.467T>C (p.Leu156Pro) n.532T>C c.53T>C (p.Leu18Pro) n.467T>C c.572T>C (p.Leu191Pro) | ClinVar dbSNP gnomAD v4 |
| 17 | g.75727853T>G | CA401039255 | ITGB4 | c.467T>G (p.Leu156Arg) n.532T>G c.53T>G (p.Leu18Arg) n.467T>G c.572T>G (p.Leu191Arg) | |
| 17 | g.75727853T= | CA2275653900 | ITGB4 | c.467T= (p.Leu156=) n.532T= c.53T= (p.Leu18=) n.467T= c.572T= (p.Leu191=) | |
| 17 | g.75727854G>A | CA501832238 | ITGB4 | c.468G>A (p.Leu156=) n.533G>A c.54G>A (p.Leu18=) n.468G>A c.573G>A (p.Leu191=) | |
| 17 | g.75727854G>C | CA501832239 | ITGB4 | c.468G>C (p.Leu156=) n.533G>C c.54G>C (p.Leu18=) n.468G>C c.573G>C (p.Leu191=) | |
| 17 | g.75727854G>T | CA501832240 | ITGB4 | c.468G>T (p.Leu156=) n.533G>T c.54G>T (p.Leu18=) n.468G>T c.573G>T (p.Leu191=) | |
| 17 | g.75727855G>A | CA401039262 | ITGB4 | c.469G>A (p.Ala157Thr) n.534G>A c.55G>A (p.Ala19Thr) n.469G>A c.574G>A (p.Ala192Thr) | gnomAD v4 |
| 17 | g.75727855G>C | CA401039260 | ITGB4 | c.469G>C (p.Ala157Pro) n.534G>C c.55G>C (p.Ala19Pro) n.469G>C c.574G>C (p.Ala192Pro) | |
| 17 | g.75727855G>T | CA401039258 | ITGB4 | c.469G>T (p.Ala157Ser) n.534G>T c.55G>T (p.Ala19Ser) n.469G>T c.574G>T (p.Ala192Ser) | |
| 17 | g.75727856G>A | CA401039266 | ITGB4 | c.469+1G>A (n.469+1G>A) n.534+1G>A c.55+1G>A (n.55+1G>A) n.469+1G>A c.574+1G>A (n.574+1G>A) | ClinVar |
| 17 | g.75727856G>C | CA8768663 | ITGB4 | c.469+1G>C (n.469+1G>C) n.534+1G>C c.55+1G>C (n.55+1G>C) n.469+1G>C c.574+1G>C (n.574+1G>C) | dbSNP ExAC gnomAD v2 |
| 17 | g.75727856G= | CA2275653901 | ITGB4 | c.469+1G= (n.469+1G=) n.534+1G= c.55+1G= (n.55+1G=) n.469+1G= c.574+1G= (n.574+1G=) | |
| 17 | g.75727856G>T | CA401039269 | ITGB4 | c.469+1G>T (n.469+1G>T) n.534+1G>T c.55+1G>T (n.55+1G>T) n.469+1G>T c.574+1G>T (n.574+1G>T) | |
| 17 | g.75727857_75727877dup | CA2697555132 | ITGB4 | c.469+2_469+22dup (n.469+2_469+22dup) n.534+2_534+22dup c.55+2_55+22dup (n.55+2_55+22dup) n.469+2_469+22dup c.574+2_574+22dup (n.574+2_574+22dup) | ClinVar |
| 17 | g.75727857T>A | CA401039273 | ITGB4 | c.469+2T>A (n.469+2T>A) n.534+2T>A c.55+2T>A (n.55+2T>A) n.469+2T>A c.574+2T>A (n.574+2T>A) | |
| 17 | g.75727857T>C | CA401039276 | ITGB4 | c.469+2T>C (n.469+2T>C) n.534+2T>C c.55+2T>C (n.55+2T>C) n.469+2T>C c.574+2T>C (n.574+2T>C) | gnomAD v4 |
| 17 | g.75727857T>G | CA401039278 | ITGB4 | c.469+2T>G (n.469+2T>G) n.534+2T>G c.55+2T>G (n.55+2T>G) n.469+2T>G c.574+2T>G (n.574+2T>G) | |
| 17 | g.75727857T= | CA2275653902 | ITGB4 | c.469+2T= (n.469+2T=) n.534+2T= c.55+2T= (n.55+2T=) n.469+2T= c.574+2T= (n.574+2T=) | |
| 17 | g.75727858A= | CA2275653903 | ITGB4 | c.469+3A= (n.469+3A=) n.534+3A= c.55+3A= (n.55+3A=) n.469+3A= c.574+3A= (n.574+3A=) | |
| 17 | g.75727858A>G | CA2733933563 | ITGB4 | c.469+3A>G (n.469+3A>G) n.534+3A>G c.55+3A>G (n.55+3A>G) n.469+3A>G c.574+3A>G (n.574+3A>G) | dbSNP |
| 17 | g.75727858A>T | CA8768664 | ITGB4 | c.469+3A>T (n.469+3A>T) n.534+3A>T c.55+3A>T (n.55+3A>T) n.469+3A>T c.574+3A>T (n.574+3A>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 17 | g.75727860_75727880dup | CA627407753 | ITGB4 | c.469+5_469+25dup (n.469+5_469+25dup) n.534+5_534+25dup c.55+5_55+25dup (n.55+5_55+25dup) n.469+5_469+25dup c.574+5_574+25dup (n.574+5_574+25dup) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 17 | g.75727859C= | CA2275653904 | ITGB4 | c.469+4C= (n.469+4C=) n.534+4C= c.55+4C= (n.55+4C=) n.469+4C= c.574+4C= (n.574+4C=) | |
| 17 | g.75727859C>T | CA8768665 | ITGB4 | c.469+4C>T (n.469+4C>T) n.534+4C>T c.55+4C>T (n.55+4C>T) n.469+4C>T c.574+4C>T (n.574+4C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |