Product Details

SNP ID
rs202086582
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:104013354 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGAACCAAAGAATCCATGACACTCA[C/T]GGCCTCCCGGGAAAGGCTGAGGCCC
Phenotype
MIM: 300507
Polymorphism
C/T, 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_001002916.4 334 Missense Mutation ATG,GTG M103V NP_001002916.3

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