Product Details

SNP ID
rs199949100
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:1254922 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATCAGCAGATGGACTGCTCCCCCAC[A/G]GCCAGCAGCAGTGCCAGTCCTGGTG
Phenotype
MIM: 606700
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MIDN PubMed Links

Gene Details

Gene
MIDN
Gene Name
midnolin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_177401.4 1361 Silent Mutation ACA,ACG T239T NP_796375.3
XM_005259671.3 1361 Silent Mutation ACA,ACG T282T XP_005259728.1
XM_005259672.3 1361 Silent Mutation ACA,ACG T281T XP_005259729.1

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