Product Details

SNP ID

rs200642266

Assay Type

Functionally tested

NCBI dbSNP Submissions

5

Location

Chr.1:160799895 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGGTCCCAAAAATGCTCTTGCTTT[C/T]GCACGTCCCAAAGAAAATGTAACCA

Phenotype

MIM: 600684

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LY9 PubMed Links

Gene Details

Gene

LY9

Gene Name

lymphocyte antigen 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001033667.2	381	Silent Mutation	TTC,TTT	F89F	NP_001028839.1
NM_001261456.1	381	Silent Mutation	TTC,TTT	F89F	NP_001248385.1
NM_001261457.1	381	Silent Mutation	TTC,TTT	F89F	NP_001248386.1
NM_002348.3	381	Silent Mutation	TTC,TTT	F89F	NP_002339.2
XM_011509548.1	381	Silent Mutation	TTC,TTT	F136F	XP_011507850.1
XM_011509549.1	381	Silent Mutation	TTC,TTT	F136F	XP_011507851.1
XM_011509550.1	381	Silent Mutation	TTC,TTT	F136F	XP_011507852.1
XM_011509552.1	381	Silent Mutation	TTC,TTT	F136F	XP_011507854.1
XM_011509556.1	381	Silent Mutation	TTC,TTT	F136F	XP_011507858.1
XM_011509560.1	381	Silent Mutation	TTC,TTT	F136F	XP_011507862.1
XM_017001297.1	381	Silent Mutation	TTC,TTT	F136F	XP_016856786.1
XM_017001298.1	381	Silent Mutation	TTC,TTT	F136F	XP_016856787.1
XM_017001299.1	381	Silent Mutation	TTC,TTT	F136F	XP_016856788.1
XM_017001300.1	381	Silent Mutation	TTC,TTT	F103F	XP_016856789.1
XM_017001301.1	381	Silent Mutation	TTC,TTT	F89F	XP_016856790.1
XM_017001302.1	381	Silent Mutation	TTC,TTT	F136F	XP_016856791.1
XM_017001303.1	381	Silent Mutation	TTC,TTT	F136F	XP_016856792.1
XM_017001304.1	381	UTR 5			XP_016856793.1

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