Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCACAATGGCAGGGCTTTGGGCTGC[A/G]GCGGATCCGAGCCCCGGCCCGAGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 609931 MIM: 609930 MIM: 601734 | ||||||||||||||||||||
Literature Links: |
MYL6 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
MYL6 - myosin light chain 6 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
MYL6B - myosin light chain 6B | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
SMARCC2 - SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005269101.1 | 3538 | Silent Mutation | GCC,GCT | A,A 1197 | XP_005269158.1 | |
XM_005269102.1 | 3538 | Silent Mutation | GCC,GCT | A,A 1196 | XP_005269159.1 | |
XM_005269103.1 | 3538 | Silent Mutation | GCC,GCT | A,A 1165 | XP_005269160.1 | |
XM_005269104.1 | 3538 | Intron | XP_005269161.1 | |||
XM_011538693.2 | 3538 | Silent Mutation | GCC,GCT | A,A 946 | XP_011536995.1 | |
XM_017019884.1 | 3538 | Intron | XP_016875373.1 | |||
XM_017019885.1 | 3538 | Intron | XP_016875374.1 | |||
XM_017019886.1 | 3538 | Intron | XP_016875375.1 | |||
XM_017019887.1 | 3538 | Silent Mutation | GCC,GCT | A,A 915 | XP_016875376.1 |