Product Details

SNP ID

rs9568354

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:49913857 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTATGATTATTAAGGTGTTATATA[C/T]GTATTACCTTATTTAATCATAGAAT

Phenotype

MIM: 607866

Polymorphism

C/T, 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	2063	UTR 3			NP_001120954.1
NM_020456.3	2063	UTR 3			NP_065189.1
XM_017020677.1	2063	Intron			XP_016876166.1

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