Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GATTTGAGCAAGTTCCGAGCACCGA[C/T]GGCCTACAGTATTGCCAGAGAAGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614394 MIM: 612912 MIM: 191161 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IFT20 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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IFT20 - intraflagellar transport 20 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001267774.1 | 369 | Missense Mutation | ATC,GTC | I,V 99 | NP_001254703.1 | |
NM_001267775.1 | 369 | Missense Mutation | ATC,GTC | I,V 73 | NP_001254704.1 | |
NM_001267776.1 | 369 | Missense Mutation | ATC,GTC | I,V 73 | NP_001254705.1 | |
NM_001267777.1 | 369 | Missense Mutation | ATC,GTC | I,V 73 | NP_001254706.1 | |
NM_001267778.1 | 369 | Intron | NP_001254707.1 | |||
NM_174887.3 | 369 | Missense Mutation | CAT,CGT | H,R 112 | NP_777547.1 |
TMEM97 - transmembrane protein 97 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014573.2 | 369 | Intron | NP_055388.2 | |||
XM_005257965.3 | 369 | Intron | XP_005258022.1 |
TNFAIP1 - TNF alpha induced protein 1 | ||||||
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There are no transcripts associated with this gene. |