Product Details

SNP ID

rs2279541

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.7:87934864 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TCGGATGAGCTGGTCCAAGGCTCTC[C/G]GGCTGGTGTCTCTGCGTCCTTCCCA

Phenotype

MIM: 603709

Polymorphism

C/G, 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	95	Intron			NP_001311346.1
NM_001324418.1	95	Intron			NP_001311347.1
NM_001324419.1	95	Intron			NP_001311348.1
NM_001324420.1	95	Intron			NP_001311349.1
NM_001324421.1	95	Intron			NP_001311350.1
NM_004194.4	95	Intron			NP_004185.1
NM_016351.5	95	Intron			NP_057435.2
NM_021721.4	95	Intron			NP_068367.1
NM_021722.5	95	Intron			NP_068368.2
NM_021723.4	95	Intron			NP_068369.1
XM_005250445.3	95	Missense Mutation	CCG,CGG	P27R	XP_005250502.1
XM_006716028.3	95	Missense Mutation	CCG,CGG	P27R	XP_006716091.1
XM_006716029.3	95	Missense Mutation	CCG,CGG	P27R	XP_006716092.1
XM_011516318.1	95	Intron			XP_011514620.1
XM_011516319.2	95	Intron			XP_011514621.1
XM_011516320.2	95	Missense Mutation	CCG,CGG	P27R	XP_011514622.1
XM_011516321.2	95	Missense Mutation	CCG,CGG	P27R	XP_011514623.1
XM_011516322.1	95	Intron			XP_011514624.1
XM_011516323.1	95	Intron			XP_011514625.1
XM_011516324.1	95	Intron			XP_011514626.1
XM_017012329.1	95	Intron			XP_016867818.1
XM_017012330.1	95	Intron			XP_016867819.1
XM_017012331.1	95	Intron			XP_016867820.1
XM_017012332.1	95	Intron			XP_016867821.1
XM_017012333.1	95	Intron			XP_016867822.1
XM_017012334.1	95	Intron			XP_016867823.1
XM_017012335.1	95	Intron			XP_016867824.1
XM_017012336.1	95	Intron			XP_016867825.1
XM_017012337.1	95	Intron			XP_016867826.1
XM_017012338.1	95	Intron			XP_016867827.1
XM_017012339.1	95	Intron			XP_016867828.1
XM_017012340.1	95	Intron			XP_016867829.1
XM_017012341.1	95	Intron			XP_016867830.1

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