Product Details

SNP ID

rs113461882

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:96814975 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTCTTGCCTCTGCTGACAGCGTGG[C/G]CAGGCGACTGCAGTCACGTCTCCAA

Phenotype

MIM: 600066

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

EPHA6 PubMed Links

Gene Details

Gene

EPHA6

Gene Name

EPH receptor A6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080448.2	395	Missense Mutation	CCA,GCA	P118A	NP_001073917.2
NM_001278300.1	395	Intron			NP_001265229.1
NM_001278301.1	395	Missense Mutation	CCA,GCA	P118A	NP_001265230.1
NM_173655.3	395	Intron			NP_775926.1
XM_006713592.3	395	Missense Mutation	CCA,GCA	P118A	XP_006713655.1
XM_011512705.2	395	Missense Mutation	CCA,GCA	P118A	XP_011511007.1
XM_011512706.2	395	Missense Mutation	CCA,GCA	P118A	XP_011511008.1
XM_011512707.2	395	Missense Mutation	CCA,GCA	P118A	XP_011511009.1
XM_017006210.1	395	Missense Mutation	CCA,GCA	P118A	XP_016861699.1
XM_017006211.1	395	UTR 5			XP_016861700.1
XM_017006212.1	395	Intron			XP_016861701.1
XM_017006213.1	395	Intron			XP_016861702.1
XM_017006214.1	395	UTR 5			XP_016861703.1
XM_017006215.1	395	Intron			XP_016861704.1
XM_017006216.1	395	Intron			XP_016861705.1
XM_017006217.1	395	Intron			XP_016861706.1
XM_017006218.1	395	Intron			XP_016861707.1
XM_017006219.1	395	Missense Mutation	CCA,GCA	P118A	XP_016861708.1
XM_017006220.1	395	Intron			XP_016861709.1
XM_017006221.1	395	Intron			XP_016861710.1
XM_017006222.1	395	Intron			XP_016861711.1
XM_017006223.1	395	Intron			XP_016861712.1

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