Product Details

SNP ID: rs143893236
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:143382268 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCCAGACTTTCCCCTGCCTCCACCT[C/T]CCCTTGCTGGGGATGGCGACGATGC
Phenotype: MIM: 179610 MIM: 602002
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: EPHA1 PubMed Links

Gene Details

Gene: EPHA1
Gene Name: EPH receptor A1

There are no transcripts associated with this gene.

Gene: FAM131B
Gene Name: family with sequence similarity 131 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001031690.2	37	Intron			NP_001026860.2
NM_001278297.1	37	Intron			NP_001265226.1
NM_014690.4	37	Intron			NP_055505.3
XM_005250073.3	37	UTR 5			XP_005250130.1
XM_006716186.2	37	Intron			XP_006716249.1

Gene: LOC100507507
Gene Name: uncharacterized LOC100507507

There are no transcripts associated with this gene.

Gene: MIR6892
Gene Name: microRNA 6892

There are no transcripts associated with this gene.

Gene: ZYX
Gene Name: zyxin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010972.1	37	Missense Mutation	CCC,TCC	P77S	NP_001010972.1
NM_003461.4	37	Missense Mutation	CCC,TCC	P77S	NP_003452.1
XM_011516569.2	37	Missense Mutation	CCC,TCC	P77S	XP_011514871.2
XM_017012587.1	37	Missense Mutation	CCC,TCC	P136S	XP_016868076.1

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