Product Details

SNP ID

rs142656048

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:49915102 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTCAAATAATATTTTTTCAAAACC[A/C]GGTGGAGGCGTATGATAAAACTCAC

Phenotype

MIM: 607866

Polymorphism

A/C, Transversion 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	818	Silent Mutation	CCG,CCT	P145P	NP_001120954.1
NM_020456.3	818	Silent Mutation	CCG,CCT	P184P	NP_065189.1
XM_017020677.1	818	Intron			XP_016876166.1

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