Product Details

SNP ID
rs17127556
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:91780687 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATCATTATGATTTCCTTCTCCTTGC[A/G]TAAGTGGGTAAAGGTCAAGAAATGC
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TC2N PubMed Links

Gene Details

Gene
TC2N
Gene Name
tandem C2 domains, nuclear
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001128595.2 4098 UTR 3 NP_001122067.1
NM_001128596.2 4098 UTR 3 NP_001122068.1
NM_001289134.1 4098 UTR 3 NP_001276063.1
NM_152332.5 4098 UTR 3 NP_689545.1

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