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GGGACTTCCAGCAGCAAAATACTTG[C/T]AGCAACTCTCTATCCTCTCATGCAT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 602500 MIM: 601306 | |||||||||||||||||||||||
Literature Links: |
GOLGB1 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
GOLGB1 - golgin B1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256486.1 | Intron | NP_001243415.1 | ||||
NM_001256487.1 | Intron | NP_001243416.1 | ||||
NM_001256488.1 | Intron | NP_001243417.1 | ||||
NM_004487.4 | Intron | NP_004478.3 | ||||
XM_005247371.4 | Intron | XP_005247428.1 | ||||
XM_005247372.4 | Intron | XP_005247429.1 | ||||
XM_005247373.1 | Intron | XP_005247430.1 | ||||
XM_006713587.1 | Intron | XP_006713650.1 | ||||
XM_006713588.1 | Intron | XP_006713651.1 | ||||
XM_006713589.1 | Intron | XP_006713652.1 | ||||
XM_006713590.1 | Intron | XP_006713653.1 | ||||
XM_006713591.1 | Intron | XP_006713654.1 | ||||
XM_011512699.2 | Intron | XP_011511001.1 | ||||
XM_017006189.1 | Intron | XP_016861678.1 | ||||
XM_017006190.1 | Intron | XP_016861679.1 | ||||
XM_017006191.1 | Intron | XP_016861680.1 | ||||
XM_017006192.1 | Intron | XP_016861681.1 | ||||
XM_017006193.1 | Intron | XP_016861682.1 | ||||
XM_017006194.1 | Intron | XP_016861683.1 | ||||
XM_017006195.1 | Intron | XP_016861684.1 |
HCLS1 - hematopoietic cell-specific Lyn substrate 1 | ||||||
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There are no transcripts associated with this gene. |