Product Details

SNP ID
rs181267165
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:56163728 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCACAGGGGTGACCGTGCCTGGGCT[C/T]GGGGCTGTGGGGTCTGGAGGCAGGG
Phenotype
MIM: 609931 MIM: 609930 MIM: 601734
Polymorphism
C/T, 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 3646 Silent Mutation CCA,CCG P1233P XP_005269158.1
XM_005269102.1 3646 Silent Mutation CCA,CCG P1232P XP_005269159.1
XM_005269103.1 3646 Silent Mutation CCA,CCG P1201P XP_005269160.1
XM_005269104.1 3646 Silent Mutation CCA,CCG P1139P XP_005269161.1
XM_011538693.2 3646 Silent Mutation CCA,CCG P982P XP_011536995.1
XM_017019884.1 3646 Silent Mutation CCA,CCG P1117P XP_016875373.1
XM_017019885.1 3646 Silent Mutation CCA,CCG P1109P XP_016875374.1
XM_017019886.1 3646 Silent Mutation CCA,CCG P1087P XP_016875375.1
XM_017019887.1 3646 Silent Mutation CCA,CCG P951P XP_016875376.1

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