Product Details

SNP ID

rs200090293

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:104013309 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGGCCAGGTGACCAGCCTCGGTGG[C/T]GATGCGGTCCAATATGTCATGAACC

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	379	Missense Mutation	ACC,GCC	T118A	NP_001002916.3

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