Product Details

SNP ID
rs149678759
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:83112855 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGTTCCTGGTAGCACTGCTGGCT[C/T]GTGTCCTCGTCAAAAGAAAACCACC
Phenotype
MIM: 616643 MIM: 606562
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
HDGFRP3 PubMed Links

Gene Details

Gene
HDGFRP3
Gene Name
hepatoma-derived growth factor, related protein 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_016073.3 3633 Intron NP_057157.1
XM_006720554.3 3633 UTR 3 XP_006720617.1
Gene
LOC105370931
Gene Name
uncharacterized LOC105370931
There are no transcripts associated with this gene.

Gene
TM6SF1
Gene Name
transmembrane 6 superfamily member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001144903.1 3633 Missense Mutation CGT,TGT R51C NP_001138375.1
NM_023003.3 3633 Missense Mutation CGT,TGT R51C NP_075379.2
XM_011521679.2 3633 Missense Mutation CGT,TGT R51C XP_011519981.1
XM_011521680.2 3633 Missense Mutation CGT,TGT R51C XP_011519982.1
XM_017022320.1 3633 Missense Mutation CGT,TGT R51C XP_016877809.1
XM_017022321.1 3633 Missense Mutation CGT,TGT R51C XP_016877810.1
XM_017022322.1 3633 Missense Mutation CGT,TGT R51C XP_016877811.1
XM_017022323.1 3633 UTR 5 XP_016877812.1
XM_017022324.1 3633 UTR 5 XP_016877813.1
XM_017022325.1 3633 UTR 5 XP_016877814.1
XM_017022326.1 3633 UTR 5 XP_016877815.1
XM_017022327.1 3633 UTR 5 XP_016877816.1
XM_017022328.1 3633 Missense Mutation CGT,TGT R51C XP_016877817.1
XM_017022329.1 3633 Missense Mutation CGT,TGT R51C XP_016877818.1
XM_017022330.1 3633 Missense Mutation CGT,TGT R51C XP_016877819.1
XM_017022331.1 3633 Missense Mutation CGT,TGT R51C XP_016877820.1

View Full Product Details