Product Details

SNP ID
rs10852860
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:3512878 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTTTGTTAAATTCCCCCACTGAGAC[A/G]TACTGAGGTATGCGACTAACTGCTG
Phenotype
MIM: 607066
Polymorphism
A/G, Transition 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 3734 Intron NP_001164166.1
NM_001170696.1 3734 Intron NP_001164167.1
NM_001170697.1 3734 Intron NP_001164168.1
NM_001170698.1 3734 Intron NP_001164169.1
NM_001170699.1 3734 Intron NP_001164170.1
NM_001321336.1 3734 Intron NP_001308265.1
NM_001321337.1 3734 Intron NP_001308266.1
NM_032598.4 3734 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 3734 UTR 3 NP_001245134.1
NM_145068.3 3734 UTR 3 NP_659505.1

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