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GGCGAGGAGTCAAAGGAACCATAGA[C/T]AGGCTGCGGCTATTGGATACTGTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608568 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MYH14 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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MYH14 - myosin, heavy chain 14, non-muscle | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077186.1 | Intron | NP_001070654.1 | ||||
NM_001145809.1 | Intron | NP_001139281.1 | ||||
NM_024729.3 | Intron | NP_079005.3 | ||||
XM_006723386.3 | Intron | XP_006723449.1 | ||||
XM_011527320.2 | Intron | XP_011525622.1 | ||||
XM_011527321.2 | Intron | XP_011525623.1 | ||||
XM_011527323.2 | Intron | XP_011525625.1 |