Product Details

SNP ID: rs6908742
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:7590386 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCCTGGGCTGGGACCTAGATAGTCT[A/G]GATCCCGGGGAAGAGGAGGCGGCGG
Phenotype: MIM: 125647
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: DSP PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152551.3	188	Silent Mutation	CTA,CTG	L43L	NP_689764.3
XM_011514312.2	188	Intron			XP_011512614.1