Product Details

SNP ID
rs146737698
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:56163752 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCGGGGCTGTGGGGTCTGGAGGCAG[A/G]GGGGTGCCTGGGTCTGTGGAGAAAA
Phenotype
MIM: 609931 MIM: 609930 MIM: 601734
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LOC107987175 PubMed Links

Gene Details

Gene
LOC107987175
Gene Name
uncharacterized LOC107987175
There are no transcripts associated with this gene.

Gene
MYL6
Gene Name
myosin light chain 6
There are no transcripts associated with this gene.

Gene
MYL6B
Gene Name
myosin light chain 6B
There are no transcripts associated with this gene.

Gene
SMARCC2
Gene Name
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_005269101.1 3622 Silent Mutation CCC,CCT P1225P XP_005269158.1
XM_005269102.1 3622 Silent Mutation CCC,CCT P1224P XP_005269159.1
XM_005269103.1 3622 Silent Mutation CCC,CCT P1193P XP_005269160.1
XM_005269104.1 3622 Silent Mutation CCC,CCT P1131P XP_005269161.1
XM_011538693.2 3622 Silent Mutation CCC,CCT P974P XP_011536995.1
XM_017019884.1 3622 Silent Mutation CCC,CCT P1109P XP_016875373.1
XM_017019885.1 3622 Silent Mutation CCC,CCT P1101P XP_016875374.1
XM_017019886.1 3622 Silent Mutation CCC,CCT P1079P XP_016875375.1
XM_017019887.1 3622 Silent Mutation CCC,CCT P943P XP_016875376.1

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