Product Details

SNP ID

rs112927852

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:87934994 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGTCATTATTTTCGCCTTTTCTCT[C/T]CACTCCCTCCTTTCCCGGTTCCTGC

Phenotype

MIM: 603709

Polymorphism

C/T, Transition 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	225	Intron			NP_001311346.1
NM_001324418.1	225	Intron			NP_001311347.1
NM_001324419.1	225	Intron			NP_001311348.1
NM_001324420.1	225	Intron			NP_001311349.1
NM_001324421.1	225	Intron			NP_001311350.1
NM_004194.4	225	Intron			NP_004185.1
NM_016351.5	225	Intron			NP_057435.2
NM_021721.4	225	Intron			NP_068367.1
NM_021722.5	225	Intron			NP_068368.2
NM_021723.4	225	Intron			NP_068369.1
XM_005250445.3	225	Silent Mutation	CTC,CTT	L70L	XP_005250502.1
XM_006716028.3	225	Silent Mutation	CTC,CTT	L70L	XP_006716091.1
XM_006716029.3	225	Silent Mutation	CTC,CTT	L70L	XP_006716092.1
XM_011516318.1	225	Intron			XP_011514620.1
XM_011516319.2	225	Intron			XP_011514621.1
XM_011516320.2	225	Silent Mutation	CTC,CTT	L70L	XP_011514622.1
XM_011516321.2	225	Silent Mutation	CTC,CTT	L70L	XP_011514623.1
XM_011516322.1	225	Intron			XP_011514624.1
XM_011516323.1	225	Intron			XP_011514625.1
XM_011516324.1	225	Intron			XP_011514626.1
XM_017012329.1	225	Intron			XP_016867818.1
XM_017012330.1	225	Intron			XP_016867819.1
XM_017012331.1	225	Intron			XP_016867820.1
XM_017012332.1	225	Intron			XP_016867821.1
XM_017012333.1	225	Intron			XP_016867822.1
XM_017012334.1	225	Intron			XP_016867823.1
XM_017012335.1	225	Intron			XP_016867824.1
XM_017012336.1	225	Intron			XP_016867825.1
XM_017012337.1	225	Intron			XP_016867826.1
XM_017012338.1	225	Intron			XP_016867827.1
XM_017012339.1	225	Intron			XP_016867828.1
XM_017012340.1	225	Intron			XP_016867829.1
XM_017012341.1	225	Intron			XP_016867830.1

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