Product Details

SNP ID

rs140608295

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:133842097 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCCTGAGCTGAGACATCTGTAAGA[C/T]GGGATATGCTGCAGGGGACAGAGGA

Phenotype

MIM: 609805

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SPATA19 PubMed Links

Gene Details

Gene

SPATA19

Gene Name

spermatogenesis associated 19

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001291992.1	538	Missense Mutation	CAT,CGT	H149R	NP_001278921.1
NM_174927.2	538	Missense Mutation	CAT,CGT	H149R	NP_777587.1

View Full Product Details