Product Details

SNP ID
rs6681025
Assay Type
Functionally tested
NCBI dbSNP Submissions
71
Location
Chr.1:84926641 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTCATTTGGGGTTCCTCTGCTCAGC[C/T]GCTGGATAAGGATGCCTGAACTTTA
Phenotype
MIM: 607399
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MCOLN2 PubMed Links

Gene Details

Gene
MCOLN2
Gene Name
mucolipin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_153259.3 1829 UTR 3 NP_694991.2
XM_005270719.3 1829 UTR 3 XP_005270776.1
XM_006710552.2 1829 UTR 3 XP_006710615.1
XM_011541187.2 1829 UTR 3 XP_011539489.1
XM_011541188.2 1829 UTR 3 XP_011539490.1
XM_017000923.1 1829 Intron XP_016856412.1

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