Product Details

SNP ID
rs149807446
Assay Type
Functionally tested
NCBI dbSNP Submissions
15
Location
Chr.1:161100735 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCCTTAGCCCCAGCCCCTTCTGAG[C/T]TTTCCTTGGCTGCTGGCTTCTCATC
Phenotype
MIM: 613466
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
KLHDC9 PubMed Links

Gene Details

Gene
KLHDC9
Gene Name
kelch domain containing 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001007255.2 476 Intron NP_001007256.1
NM_152366.4 476 Intron NP_689579.3
Gene
PFDN2
Gene Name
prefoldin subunit 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_012394.3 476 Missense Mutation NP_036526.2
XM_011509624.2 476 Missense Mutation XP_011507926.1

View Full Product Details