Product Details

SNP ID

rs6740465

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:218884873 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGTGGAATATCTGGGTGCTGACCCC[C/T]TTTCTGACCCATGTTATCAATGGGT

Phenotype

MIM: 606268

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

WNT10A PubMed Links

Gene Details

Gene

WNT10A

Gene Name

Wnt family member 10A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_025216.2		Intron			NP_079492.2
XM_011511929.2		Intron			XP_011510231.1
XM_011511930.1		Intron			XP_011510232.1

View Full Product Details