Product Details

SNP ID
rs972158
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:26295387 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGATTTCATATTCATCTGCAAAAGT[G/T]CATTATTCTGGGGGAGAGAATCTGT
Phenotype
MIM: 614780
Polymorphism
G/T, 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 Intron NP_001186764.1
NM_001199837.1 Intron NP_001186766.1
NM_001199838.1 Intron NP_001186767.1
NM_001318198.1 Intron NP_001305127.1
NM_001318199.1 Intron NP_001305128.1
NM_013322.2 Intron NP_037454.2
XM_006715712.2 Intron XP_006715775.1
XM_017012085.1 Intron XP_016867574.1
XM_017012086.1 Intron XP_016867575.1
XM_017012087.1 Intron XP_016867576.1
XM_017012088.1 Intron XP_016867577.1

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