Product Details

SNP ID: rs1188394
Assay Type: Functionally tested
NCBI dbSNP Submissions: 74
Location: Chr.1:30711371 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCTGTCAGTAGACCATGGCTGCCCT[A/C]GGGAGATGCTGGTTTTCATTTACAA
Phenotype: MIM: 115437
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: MATN1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002379.3	3736	UTR 3			NP_002370.1

There are no transcripts associated with this gene.