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GGACAGTTTTAGGTGAATGCTTGCT[C/T]TTATTGGAAGTTCTGGTTGATTTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 180385 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LMO2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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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LMO2 - LIM domain only 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142315.1 | Intron | NP_001135787.1 | ||||
NM_001142316.1 | Intron | NP_001135788.1 | ||||
NM_005574.3 | Intron | NP_005565.2 | ||||
XM_005252921.2 | Intron | XP_005252978.1 | ||||
XM_017017727.1 | Intron | XP_016873216.1 | ||||
XM_017017728.1 | Intron | XP_016873217.1 | ||||
XM_017017729.1 | Intron | XP_016873218.1 | ||||
XM_017017730.1 | Intron | XP_016873219.1 | ||||
XM_017017731.1 | Intron | XP_016873220.1 | ||||
XM_017017732.1 | Intron | XP_016873221.1 | ||||
XM_017017733.1 | Intron | XP_016873222.1 |