Product Details

SNP ID

rs201972241

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:87934479 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACGGCAGCACCATGCAGGCGGCAG[G/T]GGCTGTGTCCGTGCCCTTCTTGCTG

Phenotype

MIM: 603709

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

ADAM22 PubMed Links

Gene Details

Gene

ADAM22

Gene Name

ADAM metallopeptidase domain 22

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001324417.1	229	Missense Mutation	GGG,GTG	G5V	NP_001311346.1
NM_001324418.1	229	Missense Mutation	GGG,GTG	G5V	NP_001311347.1
NM_001324419.1	229	Missense Mutation	GGG,GTG	G5V	NP_001311348.1
NM_001324420.1	229	Missense Mutation	GGG,GTG	G5V	NP_001311349.1
NM_001324421.1	229	Missense Mutation	GGG,GTG	G5V	NP_001311350.1
NM_004194.4	229	Missense Mutation	GGG,GTG	G5V	NP_004185.1
NM_016351.5	229	Missense Mutation	GGG,GTG	G5V	NP_057435.2
NM_021721.4	229	Missense Mutation	GGG,GTG	G5V	NP_068367.1
NM_021722.5	229	Missense Mutation	GGG,GTG	G5V	NP_068368.2
NM_021723.4	229	Missense Mutation	GGG,GTG	G5V	NP_068369.1
XM_005250445.3	229	Intron			XP_005250502.1
XM_006716028.3	229	Intron			XP_006716091.1
XM_006716029.3	229	Intron			XP_006716092.1
XM_011516318.1	229	Missense Mutation	GGG,GTG	G5V	XP_011514620.1
XM_011516319.2	229	Missense Mutation	GGG,GTG	G5V	XP_011514621.1
XM_011516320.2	229	Intron			XP_011514622.1
XM_011516321.2	229	Intron			XP_011514623.1
XM_011516322.1	229	Missense Mutation	GGG,GTG	G5V	XP_011514624.1
XM_011516323.1	229	Missense Mutation	GGG,GTG	G5V	XP_011514625.1
XM_011516324.1	229	Intron			XP_011514626.1
XM_017012329.1	229	Missense Mutation	GGG,GTG	G5V	XP_016867818.1
XM_017012330.1	229	Missense Mutation	GGG,GTG	G5V	XP_016867819.1
XM_017012331.1	229	Missense Mutation	GGG,GTG	G5V	XP_016867820.1
XM_017012332.1	229	Missense Mutation	GGG,GTG	G5V	XP_016867821.1
XM_017012333.1	229	Missense Mutation	GGG,GTG	G5V	XP_016867822.1
XM_017012334.1	229	Missense Mutation	GGG,GTG	G5V	XP_016867823.1
XM_017012335.1	229	Missense Mutation	GGG,GTG	G5V	XP_016867824.1
XM_017012336.1	229	Missense Mutation	GGG,GTG	G5V	XP_016867825.1
XM_017012337.1	229	Missense Mutation	GGG,GTG	G5V	XP_016867826.1
XM_017012338.1	229	Missense Mutation	GGG,GTG	G5V	XP_016867827.1
XM_017012339.1	229	Missense Mutation	GGG,GTG	G5V	XP_016867828.1
XM_017012340.1	229	Intron			XP_016867829.1
XM_017012341.1	229	Intron			XP_016867830.1

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