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CAAGAAAATATGAGGCCTTGGACAA[C/T]GGGCAGTGCAGGACAGTGATCTCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600660 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LYSMD4 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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LYSMD4 - LysM domain containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001284417.1 | Intron | NP_001271346.1 | ||||
NM_001284418.1 | Intron | NP_001271347.1 | ||||
NM_001284419.1 | Intron | NP_001271348.1 | ||||
NM_001284420.1 | Intron | NP_001271349.1 | ||||
NM_001284421.1 | Intron | NP_001271350.1 | ||||
NM_001284422.1 | Intron | NP_001271351.1 | ||||
NM_152449.3 | Intron | NP_689662.2 | ||||
XM_006720397.3 | Intron | XP_006720460.2 | ||||
XM_011521241.1 | Intron | XP_011519543.1 | ||||
XM_011521242.2 | Intron | XP_011519544.1 | ||||
XM_011521243.2 | Intron | XP_011519545.1 | ||||
XM_011521244.1 | Intron | XP_011519546.1 | ||||
XM_011521245.2 | Intron | XP_011519547.1 | ||||
XM_017021926.1 | Intron | XP_016877415.1 | ||||
XM_017021927.1 | Intron | XP_016877416.1 | ||||
XM_017021928.1 | Intron | XP_016877417.1 | ||||
XM_017021929.1 | Intron | XP_016877418.1 | ||||
XM_017021930.1 | Intron | XP_016877419.1 |
MEF2A - myocyte enhancer factor 2A | ||||||
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There are no transcripts associated with this gene. |