Product Details

SNP ID

rs4899476

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.14:73718236 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

AGTACCTGCCGCGGCCTCCCTCCCA[A/G]GGAGGAGGTGGCCACTCAGGACACG

Phenotype

MIM: 604010

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

ELMSAN1 PubMed Links

Additional Information

For this assay, SNP(s) [rs111854480] are located under a probe and SNP(s) [rs60510049] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

ELMSAN1

Gene Name

ELM2 and Myb/SANT domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001043318.2	4607	UTR 3			NP_001036783.1
NM_194278.3	4607	UTR 3			NP_919254.2
XM_005268204.1	4607	UTR 3			XP_005268261.1
XM_005268205.1	4607	UTR 3			XP_005268262.1
XM_005268206.1	4607	UTR 3			XP_005268263.1

Gene

PNMA1

Gene Name

paraneoplastic Ma antigen 1

There are no transcripts associated with this gene.

View Full Product Details