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GTAATAGTCCTGATAACTTTACATT[A/C]TGATTAGAGGCAGCACTCTCTATAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 601907 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NEO1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
NEO1 - neogenin 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001172623.1 | Intron | NP_001166094.1 | ||||
NM_001172624.1 | Intron | NP_001166095.1 | ||||
NM_002499.3 | Intron | NP_002490.2 | ||||
XM_005254408.1 | Intron | XP_005254465.1 | ||||
XM_011521628.2 | Intron | XP_011519930.1 | ||||
XM_011521629.2 | Intron | XP_011519931.1 | ||||
XM_011521630.2 | Intron | XP_011519932.1 | ||||
XM_011521632.2 | Intron | XP_011519934.1 | ||||
XM_011521633.2 | Intron | XP_011519935.1 | ||||
XM_017022231.1 | Intron | XP_016877720.1 | ||||
XM_017022232.1 | Intron | XP_016877721.1 | ||||
XM_017022233.1 | Intron | XP_016877722.1 | ||||
XM_017022234.1 | Intron | XP_016877723.1 | ||||
XM_017022235.1 | Intron | XP_016877724.1 | ||||
XM_017022236.1 | Intron | XP_016877725.1 | ||||
XM_017022237.1 | Intron | XP_016877726.1 | ||||
XM_017022238.1 | Intron | XP_016877727.1 |