Product Details

SNP ID
rs199719028
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.21:36394597 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTTGCTGGGCAACTGATGGGAATT[C/T]AATGGCTTCTGCCTCTGTGGATAAC
Phenotype
MIM: 601245
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CHAF1B PubMed Links

Gene Details

Gene
CHAF1B
Gene Name
chromatin assembly factor 1 subunit B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005441.2 602 Intron NP_005432.1
XM_011529755.2 602 UTR 5 XP_011528057.1
XM_017028477.1 602 Missense Mutation TCA,TTA S143L XP_016883966.1
XM_017028478.1 602 Missense Mutation TCA,TTA S143L XP_016883967.1

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