Product Details

SNP ID: rs148775301
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.12:56468614 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAGATGGCGCTGCTTTTTGCACGTT[A/C]TTTGCGCTTGTGCCGCTGGGGAGCC
Phenotype: MIM: 606365
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: GLS2 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_207344.3	98	Missense Mutation	TAT,TCT	Y8S	NP_997227.1