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SNP ID: rs140321393
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:19147128 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCCAAGCCCACTGGGGTCACAGCCT[A/G]GTGGCGGTAAGGCCCCGTATACCAC
Phenotype: MIM: 600661
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: BORCS8-MEF2B PubMed Links

Gene Details

Gene: BORCS8-MEF2B
Gene Name: BORCS8-MEF2B readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005919.3	1176	Missense Mutation	CCA,CTA	P150L	NP_005910.1

Gene: MEF2B
Gene Name: myocyte enhancer factor 2B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145785.1	1176	Missense Mutation	CCA,CTA	P150L	NP_001139257.1

Gene: TMEM161A
Gene Name: transmembrane protein 161A

There are no transcripts associated with this gene.

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