Product Details

SNP ID

rs11102480

Assay Type

Functionally tested

NCBI dbSNP Submissions

15

Location

Chr.1:112481415 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAGAAGAAACTTACCCTAAAATAAT[A/C]AAGGCCATTATGAAAAGTCCACAGC

Phenotype

MIM: 601968

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

WNT2B PubMed Links

Gene Details

Gene

WNT2B

Gene Name

Wnt family member 2B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001291880.1		Intron			NP_001278809.1
NM_004185.4		Intron			NP_004176.2
NM_024494.2		Intron			NP_078613.1

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