Product Details

SNP ID

rs140231408

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:21594616 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCGGACTCGGGCGCCGGCCTCGAG[C/G]TGGGAATCGCCTCCTCCCCCACGCC

Phenotype

MIM: 184430

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SOX4 PubMed Links

Gene Details

Gene

SOX4

Gene Name

SRY-box 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003107.2	876	Missense Mutation	CTG,GTG	L28V	NP_003098.1

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