Product Details

SNP ID
rs201961449
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:85695421 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCGTGCCTGGCCCAGGAGGGCCCC[C/G]AGGTACGTGTTGGCTCTCTGCTCAC
Phenotype
MIM: 188855
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
GNLY PubMed Links

Gene Details

Gene
GNLY
Gene Name
granulysin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001302758.1 296 Missense Mutation CAG,GAG Q79E NP_001289687.1
NM_006433.4 296 Missense Mutation CAG,GAG Q52E NP_006424.2
NM_012483.3 296 Missense Mutation CAG,GAG Q37E NP_036615.2
XM_005264084.2 296 Missense Mutation CAG,GAG Q79E XP_005264141.1
XM_005264085.2 296 Missense Mutation CAG,GAG Q52E XP_005264142.1
XM_005264087.2 296 Missense Mutation CAG,GAG Q37E XP_005264144.1

View Full Product Details