Product Details

SNP ID

rs11559022

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:149968486 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATCACTGAGCATTTCTTCGCGCCA[A/G]GAGTCAAACCGTTGGTAAAGAAACC

Phenotype

MIM: 176590 MIM: 609247

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

LOC646903 PubMed Links

Gene Details

Gene

LOC646903

Gene Name

uncharacterized LOC646903

There are no transcripts associated with this gene.

Gene

PFN2

Gene Name

profilin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002628.4	295	Missense Mutation	CCT,CTT	P66L	NP_002619.1
NM_053024.3	295	Missense Mutation	CCT,CTT	P66L	NP_444252.1

Gene

RNF13

Gene Name

ring finger protein 13

There are no transcripts associated with this gene.

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