Product Details

SNP ID
rs145816840
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:44883112 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGTTGTGGCCCTGGGGGTGCTGGA[C/T]GGTGGGGTGTGTGGCTGCCACTGAG
Phenotype
MIM: 616727
Polymorphism
C/T, 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 1721 Missense Mutation NP_001129334.1
NM_001242450.1 1721 Missense Mutation NP_001229379.1
NM_001284296.1 1721 Missense Mutation NP_001271225.1
NM_138415.4 1721 Missense Mutation NP_612424.1
XM_006724122.1 1721 Missense Mutation XP_006724185.1
XM_011529855.1 1721 Intron XP_011528157.1

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