Product Details

SNP ID
rs151167617
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:8421879 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTGCTGCCACCTCCCCGGCTCCCT[G/T]TGTGACTGCTCCGGCAGCCCTGCCT
Phenotype
MIM: 613332
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
MARCH2 PubMed Links

Gene Details

Gene
MARCH2
Gene Name
membrane associated ring-CH-type finger 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001005415.1 209 Silent Mutation CTG,CTT L13L NP_001005415.1
NM_001005416.1 209 Silent Mutation CTG,CTT L13L NP_001005416.1
NM_016496.4 209 Silent Mutation CTG,CTT L13L NP_057580.3
XM_006722763.3 209 Silent Mutation CTG,CTT L13L XP_006722826.1
XM_011528046.2 209 Silent Mutation CTG,CTT L13L XP_011526348.1
XM_011528047.2 209 Silent Mutation CTG,CTT L13L XP_011526349.1
XM_017026853.1 209 Silent Mutation CTG,CTT L13L XP_016882342.1
XM_017026854.1 209 Intron XP_016882343.1

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