Product Details

SNP ID

rs104894958

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.Y:2787327 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCATTTTCCACTGGTATCCCAGCT[G/A]CTTGCTGATCTCTGAGTTTCGCATT

Phenotype

MIM: 480000

Polymorphism

G/A, Transition substitution

Allele Nomenclature

Literature Links

SRY PubMed Links

Gene Details

Gene

SRY

Gene Name

sex determining region Y

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003140.2	415	Nonsense Mutation	CAG,TAG	Q93*	NP_003131.1

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