Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.59443723_59443729dupCA599807499OR5A1c.555_561dup (p.Leu188ThrfsTer9)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.59443726A>CCA474822512OR5A1c.558A>C (p.Pro186=)
gnomAD v4
11g.59443726A>GCA474822513OR5A1c.558A>G (p.Pro186=)
11g.59443726A>TCA474822511OR5A1c.558A>T (p.Pro186=)
11g.59443727G>ACA380775166OR5A1c.559G>A (p.Val187Ile)
11g.59443727G>CCA380775181OR5A1c.559G>C (p.Val187Leu)
gnomAD v4
11g.59443727G>TCA380775193OR5A1c.559G>T (p.Val187Phe)
11g.59443728T>ACA380775196OR5A1c.560T>A (p.Val187Asp)
11g.59443728T>CCA380775199OR5A1c.560T>C (p.Val187Ala)
dbSNP gnomAD v2 gnomAD v4
11g.59443728T>GCA380775202OR5A1c.560T>G (p.Val187Gly)
11g.59443728T=CA1976399084OR5A1c.560T= (p.Val187=)
11g.59443729C>ACA474822516OR5A1c.561C>A (p.Val187=)
11g.59443729C>GCA474822514OR5A1c.561C>G (p.Val187=)
11g.59443729C>TCA474822515OR5A1c.561C>T (p.Val187=)
gnomAD v4
11g.59443730C>ACA380775203OR5A1c.562C>A (p.Leu188Met)
11g.59443730C=CA1976399087OR5A1c.562C= (p.Leu188=)
11g.59443730C>GCA380775204OR5A1c.562C>G (p.Leu188Val)
11g.59443730C>TCA474822518OR5A1c.562C>T (p.Leu188=)
dbSNP gnomAD v2 gnomAD v4 COSMIC
11g.59443731T>ACA380775216OR5A1c.563T>A (p.Leu188Gln)
11g.59443731T>CCA380775212OR5A1c.563T>C (p.Leu188Pro)
dbSNP
11g.59443731T>GCA380775205OR5A1c.563T>G (p.Leu188Arg)
11g.59443731T=CA1976399090OR5A1c.563T= (p.Leu188=)
11g.59443732G>ACA474822520OR5A1c.564G>A (p.Leu188=)
11g.59443732G>CCA474822521OR5A1c.564G>C (p.Leu188=)
11g.59443732G>TCA474822519OR5A1c.564G>T (p.Leu188=)
gnomAD v4
11g.59443733G>ACA380775217OR5A1c.565G>A (p.Ala189Thr)
gnomAD v4
11g.59443733G>CCA380775220OR5A1c.565G>C (p.Ala189Pro)
11g.59443733G>TCA380775247OR5A1c.565G>T (p.Ala189Ser)
gnomAD v4
11g.59443734C>ACA380775250OR5A1c.566C>A (p.Ala189Asp)
11g.59443734C=CA1976399092OR5A1c.566C= (p.Ala189=)
11g.59443734C>GCA380775251OR5A1c.566C>G (p.Ala189Gly)
11g.59443734C>TCA223220867OR5A1c.566C>T (p.Ala189Val)
dbSNP gnomAD v2 gnomAD v4
11g.59443735T>ACA474822525OR5A1c.567T>A (p.Ala189=)
11g.59443735T>CCA474822524OR5A1c.567T>C (p.Ala189=)
11g.59443735T>GCA474822522OR5A1c.567T>G (p.Ala189=)
11g.59443736C>ACA380775263OR5A1c.568C>A (p.Leu190Met)
11g.59443736C>GCA380775273OR5A1c.568C>G (p.Leu190Val)
11g.59443736C>TCA474822526OR5A1c.568C>T (p.Leu190=)
11g.59443737T>ACA380775277OR5A1c.569T>A (p.Leu190Gln)
11g.59443737T>CCA380775281OR5A1c.569T>C (p.Leu190Pro)
11g.59443737T>GCA380775291OR5A1c.569T>G (p.Leu190Arg)
11g.59443738G>ACA6018378OR5A1c.570G>A (p.Leu190=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.59443738G>CCA474822528OR5A1c.570G>C (p.Leu190=)
11g.59443738G=CA1976399096OR5A1c.570G= (p.Leu190=)
11g.59443738G>TCA474822529OR5A1c.570G>T (p.Leu190=)
11g.59443739T>ACA380775301OR5A1c.571T>A (p.Ser191Thr)
11g.59443739T>CCA380775302OR5A1c.571T>C (p.Ser191Pro)
COSMIC
11g.59443739T>GCA380775300OR5A1c.571T>G (p.Ser191Ala)
11g.59443740C>ACA380775303OR5A1c.572C>A (p.Ser191Tyr)
11g.59443740C=CA1976399098OR5A1c.572C= (p.Ser191=)

Number of alleles fetched