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TAAGGTAACAATCAGTTTAACAAAG[C/T]GAACTGCCAGGCACAGTGGCTCACG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
11 submissions
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Phenotype: |
MIM: 610393 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GON4L 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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GON4L - gon-4 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282856.1 | Intron | NP_001269785.1 | ||||
NM_001282858.1 | Intron | NP_001269787.1 | ||||
NM_001282860.1 | Intron | NP_001269789.1 | ||||
NM_001282861.1 | Intron | NP_001269790.1 | ||||
NM_032292.5 | Intron | NP_115668.4 | ||||
XM_005245284.3 | Intron | XP_005245341.1 | ||||
XM_005245286.3 | Intron | XP_005245343.1 | ||||
XM_006711393.3 | Intron | XP_006711456.1 | ||||
XM_006711394.3 | Intron | XP_006711457.1 | ||||
XM_011509658.2 | Intron | XP_011507960.1 | ||||
XM_011509659.2 | Intron | XP_011507961.1 |