Product Details

SNP ID

rs692274

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:49861062 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTTTTAATGTTTTTAAGACTCACC[A/G]CCCTTTATCATGGTGTCTGCACAGT

Phenotype

MIM: 611108 MIM: 608498

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

VWC2 PubMed Links

Gene Details

Gene

VWC2

Gene Name

von Willebrand factor C domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198570.4		Intron			NP_940972.2

Gene

ZPBP

Gene Name

zona pellucida binding protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001159878.1		Intron			NP_001153350.1
NM_007009.2		Intron			NP_008940.2
XM_011515095.2		Intron			XP_011513397.1
XM_011515096.2		Intron			XP_011513398.1
XM_011515097.1		Intron			XP_011513399.1
XM_011515100.2		Intron			XP_011513402.1
XM_011515101.2		Intron			XP_011513403.1
XM_011515102.2		Intron			XP_011513404.1
XM_011515103.1		Intron			XP_011513405.1
XM_017011707.1		Intron			XP_016867196.1

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