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