Product Details

SNP ID
rs75372730
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:3513932 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTTCCGCTTCTACACCGAGGTTTC[A/C]GGGAATTCCTCGACTTCTTCAAATG
Phenotype
MIM: 607066
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
SPATA22 PubMed Links

Gene Details

Gene
SPATA22
Gene Name
spermatogenesis associated 22
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001170695.1 2680 Intron NP_001164166.1
NM_001170696.1 2680 Intron NP_001164167.1
NM_001170697.1 2680 Intron NP_001164168.1
NM_001170698.1 2680 Intron NP_001164169.1
NM_001170699.1 2680 Intron NP_001164170.1
NM_001321336.1 2680 Intron NP_001308265.1
NM_001321337.1 2680 Intron NP_001308266.1
NM_032598.4 2680 Intron NP_115987.2
Gene
TRPV3
Gene Name
transient receptor potential cation channel subfamily V member 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001258205.1 2680 Silent Mutation NP_001245134.1
NM_145068.3 2680 Silent Mutation NP_659505.1

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