Product Details

SNP ID

hCV27855866

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:106308385 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGACTCCTGACTCCCAATTATTTTA[A/G]TCTTTGCACTTTTCTGCCTTGTTAA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TCP11L2 PubMed Links

Gene Details

Gene

TCP11L2

Gene Name

t-complex 11 like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286262.1		Intron			NP_001273191.1
NM_152772.2		Intron			NP_689985.1

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