Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606867 MIM: 611430 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
GORASP1 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
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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GORASP1 - golgi reassembly stacking protein 1 | ||||||
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There are no transcripts associated with this gene. |
TTC21A - tetratricopeptide repeat domain 21A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001105513.2 | 399 | Missense Mutation | CAA,CGA | Q,R 91 | NP_001098983.2 | |
NM_145755.2 | 399 | Missense Mutation | CAA,CGA | Q,R 91 | NP_665698.2 | |
XM_005264921.4 | 399 | Missense Mutation | CAA,CGA | Q,R 91 | XP_005264978.1 | |
XM_005264922.4 | 399 | Missense Mutation | CAA,CGA | Q,R 91 | XP_005264979.1 | |
XM_005264923.3 | 399 | Missense Mutation | CAA,CGA | Q,R 91 | XP_005264980.1 | |
XM_005264924.4 | 399 | Missense Mutation | CAA,CGA | Q,R 91 | XP_005264981.1 | |
XM_005264925.4 | 399 | Missense Mutation | CAA,CGA | Q,R 91 | XP_005264982.1 | |
XM_005264926.4 | 399 | Missense Mutation | CAA,CGA | Q,R 91 | XP_005264983.1 | |
XM_005264927.4 | 399 | Intron | XP_005264984.1 | |||
XM_006713011.3 | 399 | Missense Mutation | CAA,CGA | Q,R 91 | XP_006713074.1 | |
XM_011533447.2 | 399 | Missense Mutation | CAA,CGA | Q,R 91 | XP_011531749.1 | |
XM_011533449.1 | 399 | Missense Mutation | CAA,CGA | Q,R 91 | XP_011531751.1 | |
XM_017005843.1 | 399 | Missense Mutation | CAA,CGA | Q,R 91 | XP_016861332.1 |
Set Membership: |
HapMap Validated |