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GTCACTGAGTTCTATGCGGCGAATG[C/T]GTTGTGCTACTGTGATAAATTCTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606749 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TINAG 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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TINAG - tubulointerstitial nephritis antigen | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014464.3 | 382 | Missense Mutation | GCG,GTG | A,V 79 | NP_055279.3 | |
XM_006715062.2 | 382 | Missense Mutation | GCG,GTG | A,V 61 | XP_006715125.1 | |
XM_011514497.2 | 382 | Missense Mutation | GCG,GTG | A,V 79 | XP_011512799.1 | |
XM_017010745.1 | 382 | Missense Mutation | GCG,GTG | A,V 79 | XP_016866234.1 | |
XM_017010746.1 | 382 | Intron | XP_016866235.1 | |||
XM_017010747.1 | 382 | Intron | XP_016866236.1 | |||
XM_017010748.1 | 382 | Intron | XP_016866237.1 |