Product Details

SNP ID

rs149416710

Assay Type

Functionally tested

NCBI dbSNP Submissions

11

Location

Chr.1:160796226 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGTCACACAGATGACTGGGCTCC[C/T]GGGCCTTTCTCCAGTAAGCCACAGA

Phenotype

MIM: 600684

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LOC105371470 PubMed Links

Gene Details

Gene

LOC105371470

Gene Name

uncharacterized LOC105371470

There are no transcripts associated with this gene.

Gene

LY9

Gene Name

lymphocyte antigen 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001033667.2	153	Silent Mutation	CCC,CCT	P13P	NP_001028839.1
NM_001261456.1	153	Silent Mutation	CCC,CCT	P13P	NP_001248385.1
NM_001261457.1	153	Silent Mutation	CCC,CCT	P13P	NP_001248386.1
NM_002348.3	153	Silent Mutation	CCC,CCT	P13P	NP_002339.2
XM_011509548.1	153	Missense Mutation	CCG,CTG	P5L	XP_011507850.1
XM_011509549.1	153	Missense Mutation	CCG,CTG	P5L	XP_011507851.1
XM_011509550.1	153	Missense Mutation	CCG,CTG	P5L	XP_011507852.1
XM_011509552.1	153	Missense Mutation	CCG,CTG	P5L	XP_011507854.1
XM_011509556.1	153	Missense Mutation	CCG,CTG	P5L	XP_011507858.1
XM_011509560.1	153	Missense Mutation	CCG,CTG	P5L	XP_011507862.1
XM_017001297.1	153	Missense Mutation	CCG,CTG	P5L	XP_016856786.1
XM_017001298.1	153	Missense Mutation	CCG,CTG	P5L	XP_016856787.1
XM_017001299.1	153	Missense Mutation	CCG,CTG	P5L	XP_016856788.1
XM_017001300.1	153	Missense Mutation	CCG,CTG	P5L	XP_016856789.1
XM_017001301.1	153	Silent Mutation	CCC,CCT	P13P	XP_016856790.1
XM_017001302.1	153	Missense Mutation	CCG,CTG	P5L	XP_016856791.1
XM_017001303.1	153	Missense Mutation	CCG,CTG	P5L	XP_016856792.1
XM_017001304.1	153	UTR 5			XP_016856793.1

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