Product Details

SNP ID

rs940655

Assay Type

Functionally tested

NCBI dbSNP Submissions

48

Location

Chr.1:204078173 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGGCTGATGATGTCTGCGGCAGCAG[C/T]GCTCCATGAATGGTAAGGGCTCTGG

Phenotype

MIM: 604748

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SOX13 PubMed Links

Gene Details

Gene

SOX13

Gene Name

SRY-box 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005686.2		Intron			NP_005677.2
XM_005245623.2		Intron			XP_005245680.1

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