Product Details

SNP ID

rs201166256

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:96814700 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGTCCTCCTCCGAAGCAGCTGCAC[A/C]TGCAACTGGGCAGCCTGGACCCTCG

Phenotype

MIM: 600066

Polymorphism

A/C, 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	120	Missense Mutation	CAT,CCT	H26P	NP_001073917.2
NM_001278300.1	120	Intron			NP_001265229.1
NM_001278301.1	120	Missense Mutation	CAT,CCT	H26P	NP_001265230.1
NM_173655.3	120	Intron			NP_775926.1
XM_006713592.3	120	Missense Mutation	CAT,CCT	H26P	XP_006713655.1
XM_011512705.2	120	Missense Mutation	CAT,CCT	H26P	XP_011511007.1
XM_011512706.2	120	Missense Mutation	CAT,CCT	H26P	XP_011511008.1
XM_011512707.2	120	Missense Mutation	CAT,CCT	H26P	XP_011511009.1
XM_017006210.1	120	Missense Mutation	CAT,CCT	H26P	XP_016861699.1
XM_017006211.1	120	UTR 5			XP_016861700.1
XM_017006212.1	120	Intron			XP_016861701.1
XM_017006213.1	120	Intron			XP_016861702.1
XM_017006214.1	120	UTR 5			XP_016861703.1
XM_017006215.1	120	Intron			XP_016861704.1
XM_017006216.1	120	Intron			XP_016861705.1
XM_017006217.1	120	Intron			XP_016861706.1
XM_017006218.1	120	Intron			XP_016861707.1
XM_017006219.1	120	Missense Mutation	CAT,CCT	H26P	XP_016861708.1
XM_017006220.1	120	Intron			XP_016861709.1
XM_017006221.1	120	Intron			XP_016861710.1
XM_017006222.1	120	Intron			XP_016861711.1
XM_017006223.1	120	Intron			XP_016861712.1

View Full Product Details