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TTAAAATCCCAGCAGGATTTTGAGA[A/G]AAAACTAATTCTAAAGTTAAGTTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611700 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SVOPL 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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SVOPL - SVOP like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001139456.1 | Intron | NP_001132928.1 | ||||
NM_174959.3 | Intron | NP_777619.1 | ||||
XM_005250143.3 | Intron | XP_005250200.1 | ||||
XM_011515797.2 | Intron | XP_011514099.1 | ||||
XM_017011746.1 | Intron | XP_016867235.1 | ||||
XM_017011747.1 | Intron | XP_016867236.1 | ||||
XM_017011748.1 | Intron | XP_016867237.1 |