Product Details

SNP ID

rs181119565

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:96814642 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGGTGGATGCAATTCCCCTCGCCT[C/T]CAGCCGCGAGGAGCTCCCCGGCGCC

Phenotype

MIM: 600066

Polymorphism

C/T, Transition 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	62	Missense Mutation	CCA,TCA	P7S	NP_001073917.2
NM_001278300.1	62	Intron			NP_001265229.1
NM_001278301.1	62	Missense Mutation	CCA,TCA	P7S	NP_001265230.1
NM_173655.3	62	Intron			NP_775926.1
XM_006713592.3	62	Missense Mutation	CCA,TCA	P7S	XP_006713655.1
XM_011512705.2	62	Missense Mutation	CCA,TCA	P7S	XP_011511007.1
XM_011512706.2	62	Missense Mutation	CCA,TCA	P7S	XP_011511008.1
XM_011512707.2	62	Missense Mutation	CCA,TCA	P7S	XP_011511009.1
XM_017006210.1	62	Missense Mutation	CCA,TCA	P7S	XP_016861699.1
XM_017006211.1	62	UTR 5			XP_016861700.1
XM_017006212.1	62	Intron			XP_016861701.1
XM_017006213.1	62	Intron			XP_016861702.1
XM_017006214.1	62	UTR 5			XP_016861703.1
XM_017006215.1	62	Intron			XP_016861704.1
XM_017006216.1	62	Intron			XP_016861705.1
XM_017006217.1	62	Intron			XP_016861706.1
XM_017006218.1	62	Intron			XP_016861707.1
XM_017006219.1	62	Missense Mutation	CCA,TCA	P7S	XP_016861708.1
XM_017006220.1	62	Intron			XP_016861709.1
XM_017006221.1	62	Intron			XP_016861710.1
XM_017006222.1	62	Intron			XP_016861711.1
XM_017006223.1	62	Intron			XP_016861712.1

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