Product Details

SNP ID

rs199724832

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:104013654 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGGGAAGCCGGGGCACTTCGGTAC[A/G]CAGCATGGCTCCACGTCTCGGGCCA

Phenotype

MIM: 300507

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

H2BFWT PubMed Links

Gene Details

Gene

H2BFWT

Gene Name

H2B histone family member W, testis specific

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001002916.4	34	Missense Mutation	CGT,TGT	R3C	NP_001002916.3

View Full Product Details