Product Details

SNP ID: rs16943091
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:58541892 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GTCCTCCCATCCCCCAAGCTCCCAC[A/C]GTGGGCCCATAGGAGGGAAAAGCAC
Phenotype: MIM: 603696
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: C17orf47 PubMed Links

Gene Details

Gene: C17orf47
Gene Name: chromosome 17 open reading frame 47

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001038704.2	1822	Missense Mutation	GGT,TGT	G546C	NP_001033793.2
XM_011524637.2	1822	Intron			XP_011522939.1
XM_017024498.1	1822	Intron			XP_016879987.1

Gene: SEPT4
Gene Name: septin 4

There are no transcripts associated with this gene.

Gene: SEPT4-AS1
Gene Name: SEPT4 antisense RNA 1

There are no transcripts associated with this gene.

View Full Product Details