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SNP ID

rs5975745

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:136536886 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACAAATATGCAAATTTGTGAGCACT[A/G]TATCTAGGTACAAAGAACCTTGAAA

Phenotype

MIM: 300583

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

VGLL1 PubMed Links

Gene Details

Gene

VGLL1

Gene Name

vestigial like family member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016267.3		Intron			NP_057351.1

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