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GGTCTCTGCTTTCCTGGTTCCATTC[C/T]TTCTGTCCTGTGGGCCAAGTCACAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606127 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC101928418 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) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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LOC101928418 - uncharacterized LOC101928418 | ||||||
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There are no transcripts associated with this gene. |
MYOCD - myocardin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146312.2 | Intron | NP_001139784.1 | ||||
NM_153604.3 | Intron | NP_705832.1 | ||||
XM_005256863.1 | Intron | XP_005256920.1 | ||||
XM_005256864.1 | Intron | XP_005256921.1 | ||||
XM_017025342.1 | Intron | XP_016880831.1 |