Product Details

SNP ID

rs28441357

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:117268529 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCTGCTGGGAAGGACCCATAGGGG[G/T]TCCTCTCAGCCTGGGGTTCACCTAC

Phenotype

MIM: 609979

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

VGLL2 PubMed Links

Gene Details

Gene

VGLL2

Gene Name

vestigial like family member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_153453.1		Intron			NP_703154.1
NM_182645.3		Intron			NP_872586.1
XM_005266883.2		Intron			XP_005266940.1

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