Product Details

SNP ID: rs139664603
Assay Type: Functionally tested
NCBI dbSNP Submissions: 4
Location: Chr.1:177932764 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GACTCAGGGGAAGGTGTCAGTGAGA[A/G]GCCCAGGCCAGCCTGGTGGGGAGAA
Phenotype: MIM: 612855
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: SEC16B PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033127.2	2956	Missense Mutation	CTC,TTC	L956F	NP_149118.2