Product Details

SNP ID

rs201321708

Assay Type

Functionally tested

NCBI dbSNP Submissions

6

Location

Chr.1:152972057 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCCAGGTCAAGAAGCAATGCCCAC[C/T]GAAAGGCACCATCATTCCAGCCCAG

Phenotype

MIM: 616363

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SPRR4 PubMed Links

Gene Details

Gene

SPRR4

Gene Name

small proline rich protein 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173080.2	925	Missense Mutation	CCG,CTG	P56L	NP_775103.1
XM_017000482.1	925	Missense Mutation	CCG,CTG	P56L	XP_016855971.1

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