Product Details

SNP ID

rs75423671

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.18:3266437 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATATCTTATTGTCACAATATCTTA[C/T]TGGTTACACGGGTCAACACTTTTCA

Phenotype

MIM: 609211

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

LOC104968399 PubMed Links

Additional Information

For this assay, SNP(s) [rs140337632] 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

LOC104968399

Gene Name

uncharacterized LOC104968399

There are no transcripts associated with this gene.

Gene

MYL12B

Gene Name

myosin light chain 12B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001144944.1		Intron			NP_001138416.1
NM_001144945.1		Intron			NP_001138417.1
NM_033546.3		Intron			NP_291024.1

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