Product Details

SNP ID
rs141926120
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:49914652 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGTATATAAAAAAGGACACTAAGC[A/G]GCAAAATTATCCAACTGTAGATGTC
Phenotype
MIM: 607866
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SPRYD7 PubMed Links

Gene Details

Gene
SPRYD7
Gene Name
SPRY domain containing 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001127482.2 1268 UTR 3 NP_001120954.1
NM_020456.3 1268 UTR 3 NP_065189.1
XM_017020677.1 1268 Intron XP_016876166.1

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