Product Details

SNP ID: rs16893892
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:28272095 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGCAAACAATTCAGGCAGTTGCGTT[A/G]TGAAGAGACCACAGGACCTCGAGAA
Phenotype: MIM: 616474
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: PGBD1 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_001023560.3	297	Missense Mutation	TAT,TGT	Y59C	NP_001018854.2
NM_001111039.2	297	Missense Mutation	TAT,TGT	Y59C	NP_001104509.1
NM_001287421.1	297	Intron			NP_001274350.1
NM_001287422.1	297	Intron			NP_001274351.1
NM_152736.5	297	Intron			NP_689949.3
XM_011514862.2	297	Missense Mutation	TAT,TGT	Y59C	XP_011513164.1
XM_011514864.1	297	Missense Mutation	TAT,TGT	Y30C	XP_011513166.1
XM_011514866.1	297	Intron			XP_011513168.1
XM_011514867.1	297	UTR 5			XP_011513169.1
XM_011514869.1	297	UTR 5			XP_011513171.1
XM_017011264.1	297	Missense Mutation	TAT,TGT	Y59C	XP_016866753.1
XM_017011265.1	297	UTR 5			XP_016866754.1