Product Details

SNP ID: rs199592567
Assay Type: Functionally tested
NCBI dbSNP Submissions: 7
Location: Chr.1:34988898 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TTTTTTTCTTTGAAGGTGGAGAATC[A/G]AGTTCTGCATCATTTTTTTCATTAG
Phenotype: MIM: 613567
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: TMEM35B 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_007167.3	2412	Silent Mutation	CTC,CTT	L728L	NP_009098.3