Product Details

SNP ID

rs201909222

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:153607598 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCGATGGGGCCGGTGATGCCGCCT[A/G]TCAAGGTCCAGTACTCATCGAAGCT

Phenotype

MIM: 607986

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

S100A14 PubMed Links

Gene Details

Gene

S100A14

Gene Name

S100 calcium binding protein A14

There are no transcripts associated with this gene.

Gene

S100A16

Gene Name

S100 calcium binding protein A16

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317007.1	491	Missense Mutation	ACA,ATA	T83I	NP_001303936.1
NM_001317008.1	491	Missense Mutation	ACA,ATA	T83I	NP_001303937.1
NM_080388.2	491	Missense Mutation	ACA,ATA	T83I	NP_525127.1

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