Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAGCTAGGGCTGCTGGGACCCTAAG[G/T]GGCTGCCTTCGGGATGCCGGGGCTA
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615078 MIM: 600537 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
GOLT1B 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)
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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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GOLT1B - golgi transport 1B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016072.4 | Intron | NP_057156.1 | ||||
XM_017019384.1 | Intron | XP_016874873.1 |
RECQL - RecQ like helicase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002907.3 | Intron | NP_002898.2 | ||||
NM_032941.2 | Intron | NP_116559.1 | ||||
XM_005253461.3 | Intron | XP_005253518.1 | ||||
XM_005253462.4 | Intron | XP_005253519.1 | ||||
XM_005253463.3 | Intron | XP_005253520.1 | ||||
XM_005253464.3 | Intron | XP_005253521.1 |
Set Membership: |
HapMap |