Product Details

SNP ID
rs762980
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.22:44882229 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
GTTAAGTTGAATGATTCAACCCCAA[A/G]GAGAAAACCTGCCAAATGCTGCCCC
Phenotype
MIM: 616727
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PHF21B PubMed Links

Gene Details

Gene
PHF21B
Gene Name
PHD finger protein 21B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001135862.2 2604 UTR 3 NP_001129334.1
NM_001242450.1 2604 UTR 3 NP_001229379.1
NM_001284296.1 2604 UTR 3 NP_001271225.1
NM_138415.4 2604 UTR 3 NP_612424.1
XM_006724122.1 2604 UTR 3 XP_006724185.1
XM_011529855.1 2604 Intron XP_011528157.1

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