Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.27084745G=CA1240109462EMILIN1c.2557+214G= (n.2557+214G=)
c.549+214G=
2g.27084745G>TCA1240109463EMILIN1c.2557+214G>T (n.2557+214G>T)
c.549+214G>T
 dbSNP
2g.27084746T>CCA767343369EMILIN1c.2557+215T>C (n.2557+215T>C)
c.549+215T>C
 dbSNP
2g.27084746T>GCA531422387EMILIN1c.2557+215T>G (n.2557+215T>G)
c.549+215T>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.27084746T=CA1240109464EMILIN1c.2557+215T= (n.2557+215T=)
c.549+215T=
2g.27084752C>TCA2749254978EMILIN1c.2557+221C>T (n.2557+221C>T)
c.549+221C>T
2g.27084753C=CA1240109465EMILIN1c.2557+222C= (n.2557+222C=)
c.549+222C=
2g.27084753C>TCA1028652994EMILIN1c.2557+222C>T (n.2557+222C>T)
c.549+222C>T
 dbSNP gnomAD v3 gnomAD v4
2g.27084754A=CA1240109466EMILIN1c.2557+223A= (n.2557+223A=)
c.549+223A=
2g.27084754A>GCA1240109467EMILIN1c.2557+223A>G (n.2557+223A>G)
c.549+223A>G
 dbSNP
2g.27084765G>ACA44468506EMILIN1c.2558-226G>A (n.2558-226G>A)
c.550-226G>A
 dbSNP
2g.27084765G=CA1240109468EMILIN1c.2558-226G= (n.2558-226G=)
c.550-226G=
2g.27084766G>ACA2594582120EMILIN1c.2558-225G>A (n.2558-225G>A)
c.550-225G>A
 dbSNP gnomAD v3 gnomAD v4
2g.27084767A=CA1240109469EMILIN1c.2558-224A= (n.2558-224A=)
c.550-224A=
2g.27084767A>GCA531422388EMILIN1c.2558-224A>G (n.2558-224A>G)
c.550-224A>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.27084768G>ACA2698965869EMILIN1c.2558-223G>A (n.2558-223G>A)
c.550-223G>A
 dbSNP
2g.27084772A=CA1240109470EMILIN1c.2558-219A= (n.2558-219A=)
c.550-219A=
2g.27084772A>GCA44468508EMILIN1c.2558-219A>G (n.2558-219A>G)
c.550-219A>G
 dbSNP
2g.27084773A=CA1240109471EMILIN1c.2558-218A= (n.2558-218A=)
c.550-218A=
2g.27084773A>CCA44468510EMILIN1c.2558-218A>C (n.2558-218A>C)
c.550-218A>C
 dbSNP
2g.27084775G>CCA531422389EMILIN1c.2558-216G>C (n.2558-216G>C)
c.550-216G>C
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.27084775G=CA1240109472EMILIN1c.2558-216G= (n.2558-216G=)
c.550-216G=
2g.27084778G>TCA2519869686EMILIN1c.2558-213G>T (n.2558-213G>T)
c.550-213G>T
2g.27084783T>ACA767343385EMILIN1c.2558-208T>A (n.2558-208T>A)
c.550-208T>A
 dbSNP gnomAD v3 gnomAD v4
2g.27084783T=CA1240109473EMILIN1c.2558-208T= (n.2558-208T=)
c.550-208T=
2g.27084786T>GCA44468512EMILIN1c.2558-205T>G (n.2558-205T>G)
c.550-205T>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.27084786T=CA1240109474EMILIN1c.2558-205T= (n.2558-205T=)
c.550-205T=
2g.27084793G>CCA44468514EMILIN1c.2558-198G>C (n.2558-198G>C)
c.550-198G>C
 dbSNP gnomAD v3 gnomAD v4
2g.27084793G=CA1240109475EMILIN1c.2558-198G= (n.2558-198G=)
c.550-198G=
2g.27084800G>ACA531422390EMILIN1c.2558-191G>A (n.2558-191G>A)
c.550-191G>A
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.27084800G=CA1240109476EMILIN1c.2558-191G= (n.2558-191G=)
c.550-191G=
2g.27084804G>CCA2749254979EMILIN1c.2558-187G>C (n.2558-187G>C)
c.550-187G>C
2g.27084809G>CCA767343398EMILIN1c.2558-182G>C (n.2558-182G>C)
c.550-182G>C
 dbSNP
2g.27084809G=CA1240109477EMILIN1c.2558-182G= (n.2558-182G=)
c.550-182G=
2g.27084810C>ACA1240109479EMILIN1c.2558-181C>A (n.2558-181C>A)
c.550-181C>A
 dbSNP
2g.27084810C=CA1240109478EMILIN1c.2558-181C= (n.2558-181C=)
c.550-181C=
2g.27084812G>TCA2749254980EMILIN1c.2558-179G>T (n.2558-179G>T)
c.550-179G>T
2g.27084814G>ACA1240109481EMILIN1c.2558-177G>A (n.2558-177G>A)
c.550-177G>A
 dbSNP
2g.27084814G=CA1240109480EMILIN1c.2558-177G= (n.2558-177G=)
c.550-177G=
2g.27084817G>ACA1240109482EMILIN1c.2558-174G>A (n.2558-174G>A)
c.550-174G>A
 dbSNP
2g.27084817G=CA1240109483EMILIN1c.2558-174G= (n.2558-174G=)
c.550-174G=
2g.27084817G>TCA531422391EMILIN1c.2558-174G>T (n.2558-174G>T)
c.550-174G>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.27084819C>ACA1240109485EMILIN1c.2558-172C>A (n.2558-172C>A)
c.550-172C>A
 dbSNP
2g.27084819C=CA1240109484EMILIN1c.2558-172C= (n.2558-172C=)
c.550-172C=
2g.27084820C=CA1240109486EMILIN1c.2558-171C= (n.2558-171C=)
c.550-171C=
2g.27084820C>TCA767343408EMILIN1c.2558-171C>T (n.2558-171C>T)
c.550-171C>T
 dbSNP
2g.27084821C>ACA44468516EMILIN1c.2558-170C>A (n.2558-170C>A)
c.550-170C>A
 dbSNP
2g.27084821C=CA1240109487EMILIN1c.2558-170C= (n.2558-170C=)
c.550-170C=
2g.27084823G>ACA44468518EMILIN1c.2558-168G>A (n.2558-168G>A)
c.550-168G>A
 dbSNP
2g.27084823G=CA1240109488EMILIN1c.2558-168G= (n.2558-168G=)
c.550-168G=
2g.27084824C>ACA767343412EMILIN1c.2558-167C>A (n.2558-167C>A)
c.550-167C>A
 dbSNP
2g.27084824C=CA1240109489EMILIN1c.2558-167C= (n.2558-167C=)
c.550-167C=
2g.27084826G>ACA531422392EMILIN1c.2558-165G>A (n.2558-165G>A)
c.550-165G>A
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.27084826G=CA1240109490EMILIN1c.2558-165G= (n.2558-165G=)
c.550-165G=
2g.27084831A=CA1240109491EMILIN1c.2558-160A= (n.2558-160A=)
c.550-160A=
2g.27084831A>GCA1240109492EMILIN1c.2558-160A>G (n.2558-160A>G)
c.550-160A>G
 dbSNP
2g.27084833A=CA1240109493EMILIN1c.2558-158A= (n.2558-158A=)
c.550-158A=
2g.27084833A>CCA767343422EMILIN1c.2558-158A>C (n.2558-158A>C)
c.550-158A>C
 dbSNP gnomAD v3 gnomAD v4
2g.27084834G>ACA2698966085EMILIN1c.2558-157G>A (n.2558-157G>A)
c.550-157G>A
 dbSNP
2g.27084835A>TCA2698966127EMILIN1c.2558-156A>T (n.2558-156A>T)
c.550-156A>T
 dbSNP
2g.27084837T>CCA44468519EMILIN1c.2558-154T>C (n.2558-154T>C)
c.550-154T>C
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.27084837T=CA1240109494EMILIN1c.2558-154T= (n.2558-154T=)
c.550-154T=
2g.27084839G>ACA1240109496EMILIN1c.2558-152G>A (n.2558-152G>A)
c.550-152G>A
 dbSNP
2g.27084839G=CA1240109495EMILIN1c.2558-152G= (n.2558-152G=)
c.550-152G=
2g.27084839G>TCA2658282634EMILIN1c.2558-152G>T (n.2558-152G>T)
c.550-152G>T
 gnomAD v4
2g.27084840A=CA1240109497EMILIN1c.2558-151A= (n.2558-151A=)
c.550-151A=
2g.27084840A>GCA767343432EMILIN1c.2558-151A>G (n.2558-151A>G)
c.550-151A>G
 dbSNP
2g.27084841C>ACA1240109499EMILIN1c.2558-150C>A (n.2558-150C>A)
c.550-150C>A
 dbSNP gnomAD v4
2g.27084841C=CA1240109498EMILIN1c.2558-150C= (n.2558-150C=)
c.550-150C=
2g.27084842C>ACA2658282637EMILIN1c.2558-149C>A (n.2558-149C>A)
c.550-149C>A
 gnomAD v4
2g.27084843C>ACA767343433EMILIN1c.2558-148C>A (n.2558-148C>A)
c.550-148C>A
 dbSNP gnomAD v3 gnomAD v4
2g.27084843C=CA1240109500EMILIN1c.2558-148C= (n.2558-148C=)
c.550-148C=
2g.27084844T>CCA2658282644EMILIN1c.2558-147T>C (n.2558-147T>C)
c.550-147T>C
 gnomAD v4
2g.27084845A>TCA2658282648EMILIN1c.2558-146A>T (n.2558-146A>T)
c.550-146A>T
 gnomAD v4

Number of alleles fetched