Product Details

SNP ID: rs6601645
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:11993176 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GTAAAGAAAATCATGAGTCCAAATG[C/G]ATTTAGGCAGTTTATTAGTTACACA
Phenotype
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: DEFB134 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001302695.1	1804	Intron			NP_001289624.1
XM_017013724.1	1804	UTR 3			XP_016869213.1

There are no transcripts associated with this gene.