Product Details

SNP ID

rs200296448

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:241496494 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAGGCGTTCTCCAGCTCCTCCAGC[A/G]CACCCACGCTCCCGCCGCTCTGCTT

Phenotype

MIM: 602255

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FARP2 PubMed Links

Gene Details

Gene

FARP2

Gene Name

FERM, ARH/RhoGEF and pleckstrin domain protein 2

There are no transcripts associated with this gene.

Gene

STK25

Gene Name

serine/threonine kinase 25

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271977.1	1204	Missense Mutation	GCG,GTG	A382V	NP_001258906.1
NM_001271978.1	1204	Missense Mutation	GCG,GTG	A382V	NP_001258907.1
NM_001271979.1	1204	Missense Mutation	GCG,GTG	A305V	NP_001258908.1
NM_001271980.1	1204	Missense Mutation	GCG,GTG	A305V	NP_001258909.1
NM_001282305.1	1204	Missense Mutation	GCG,GTG	A288V	NP_001269234.1
NM_001282306.1	1204	Missense Mutation	GCG,GTG	A308V	NP_001269235.1
NM_001282307.1	1204	Missense Mutation	GCG,GTG	A288V	NP_001269236.1
NM_001282308.1	1204	Missense Mutation	GCG,GTG	A288V	NP_001269237.1
NM_006374.4	1204	Missense Mutation	GCG,GTG	A382V	NP_006365.2
XM_011510493.2	1204	Intron			XP_011508795.1
XM_011510494.2	1204	Missense Mutation	GCG,GTG	A308V	XP_011508796.1
XM_011510495.2	1204	Missense Mutation	GCG,GTG	A308V	XP_011508797.1
XM_011510496.2	1204	Intron			XP_011508798.1
XM_017003168.1	1204	Missense Mutation	CGC,TGC	R344C	XP_016858657.1
XM_017003169.1	1204	Missense Mutation	CGC,TGC	R344C	XP_016858658.1
XM_017003170.1	1204	Missense Mutation	GCG,GTG	A308V	XP_016858659.1
XM_017003171.1	1204	Missense Mutation	CGC,TGC	R250C	XP_016858660.1

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