Product Details

SNP ID
rs140395242
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:44883296 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGCCAGCAGGCTTGTCTTCAACTC[C/T]AGGCATTTCTGTTGGGGAGAAGGTC
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 1537 Silent Mutation CTA,CTG L420L NP_001129334.1
NM_001242450.1 1537 Silent Mutation CTA,CTG L408L NP_001229379.1
NM_001284296.1 1537 Silent Mutation CTA,CTG L258L NP_001271225.1
NM_138415.4 1537 Silent Mutation CTA,CTG L462L NP_612424.1
XM_006724122.1 1537 Silent Mutation CTA,CTG L420L XP_006724185.1
XM_011529855.1 1537 Intron XP_011528157.1

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