Product Details

SNP ID

rs149719025

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:132333730 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGGAGGTCTTTAGAATCCCCAGCC[G/T]TCAAGTAAGTGGGGCTGCTCCTCAG

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

LRRC27 PubMed Links

Gene Details

Gene

LRRC27

Gene Name

leucine rich repeat containing 27

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001143757.1	347	Missense Mutation	CGT,CTT	R69L	NP_001137229.1
NM_001143758.1	347	Missense Mutation	CGT,CTT	R69L	NP_001137230.1
NM_001143759.1	347	Missense Mutation	CGT,CTT	R69L	NP_001137231.1
NM_001309474.1	347	Intron			NP_001296403.1
NM_030626.2	347	Missense Mutation	CGT,CTT	R69L	NP_085129.1
XM_006717983.2	347	Missense Mutation	CGT,CTT	R69L	XP_006718046.1
XM_006717984.2	347	Missense Mutation	CGT,CTT	R69L	XP_006718047.1
XM_011540208.1	347	Missense Mutation	CGT,CTT	R69L	XP_011538510.1
XM_011540209.1	347	Missense Mutation	CGT,CTT	R69L	XP_011538511.1
XM_011540210.2	347	Intron			XP_011538512.1
XM_017016690.1	347	Missense Mutation	CGT,CTT	R69L	XP_016872179.1
XM_017016691.1	347	Missense Mutation	CGT,CTT	R69L	XP_016872180.1
XM_017016692.1	347	Missense Mutation	CGT,CTT	R69L	XP_016872181.1
XM_017016693.1	347	Missense Mutation	CGT,CTT	R69L	XP_016872182.1
XM_017016694.1	347	UTR 5			XP_016872183.1

Gene

STK32C

Gene Name

serine/threonine kinase 32C

There are no transcripts associated with this gene.

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