Product Details

SNP ID
rs3829844
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:26292708 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCGTCACGGAATGGGGAGCAACATG[G/T]CCTGCTGAAAGGAAGGGCTTCTATC
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_001199835.1 147 Intron NP_001186764.1
NM_001199837.1 147 Intron NP_001186766.1
NM_001199838.1 147 Intron NP_001186767.1
NM_001318198.1 147 Intron NP_001305127.1
NM_001318199.1 147 Intron NP_001305128.1
NM_013322.2 147 Intron NP_037454.2
XM_006715712.2 147 Intron XP_006715775.1
XM_017012085.1 147 Intron XP_016867574.1
XM_017012086.1 147 UTR 5 XP_016867575.1
XM_017012087.1 147 Intron XP_016867576.1
XM_017012088.1 147 Intron XP_016867577.1

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