Product Details

SNP ID: rs4905374
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.14:95687468 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CATCCTCTACTATATTTGAAATCAG[A/G]TTACTAATAACACCTAATGCTACAC
Phenotype: MIM: 186960 MIM: 603769
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: TCL1A PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004918.3		Intron			NP_004909.1