Product Details

SNP ID
rs2698724
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:26292034 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTTTGAGTCAGCAAACTCCGCGGC[A/C]CGCAAGCCCGGCTCGGCCCGGCCCT
Phenotype
MIM: 614780
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
SNX10 PubMed Links

Gene Details

Gene
SNX10
Gene Name
sorting nexin 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199835.1 116 UTR 5 NP_001186764.1
NM_001199837.1 116 Intron NP_001186766.1
NM_001199838.1 116 Intron NP_001186767.1
NM_001318198.1 116 UTR 5 NP_001305127.1
NM_001318199.1 116 Intron NP_001305128.1
NM_013322.2 116 UTR 5 NP_037454.2
XM_006715712.2 116 Intron XP_006715775.1
XM_017012085.1 116 UTR 5 XP_016867574.1
XM_017012086.1 116 Intron XP_016867575.1
XM_017012087.1 116 UTR 5 XP_016867576.1
XM_017012088.1 116 UTR 5 XP_016867577.1

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