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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