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SNP ID

rs77211423

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:74317443 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGATGCTATTGTCTTCTAGTGAGT[A/G]CTGCAAAGTATCCTACAATAATGCA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

VRTN PubMed Links

Gene Details

Gene

VRTN

Gene Name

vertebrae development associated

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018228.2		Intron			NP_060698.2
XM_011536911.1		Intron			XP_011535213.1

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