Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611143 MIM: 606769 MIM: 611983 | ||||||||||||||||||||
Literature Links: |
FAM175A PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | 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 |
FAM175A - family with sequence similarity 175 member A | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
HELQ - helicase, POLQ-like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001297755.1 | 165 | Intron | NP_001284684.1 | |||
NM_001297756.1 | 165 | Intron | NP_001284685.1 | |||
NM_001297757.1 | 165 | Intron | NP_001284686.1 | |||
NM_001297758.1 | 165 | Intron | NP_001284687.1 | |||
NM_001297759.1 | 165 | Intron | NP_001284688.1 | |||
NM_133636.3 | 165 | Intron | NP_598375.2 | |||
XM_005262711.1 | 165 | Intron | XP_005262768.1 | |||
XM_005262713.2 | 165 | Intron | XP_005262770.1 | |||
XM_006714076.2 | 165 | Intron | XP_006714139.1 | |||
XM_011531580.2 | 165 | Intron | XP_011529882.1 | |||
XM_017007679.1 | 165 | Intron | XP_016863168.1 | |||
XM_017007680.1 | 165 | Intron | XP_016863169.1 | |||
XM_017007681.1 | 165 | Intron | XP_016863170.1 | |||
XM_017007682.1 | 165 | Intron | XP_016863171.1 | |||
XM_017007683.1 | 165 | Intron | XP_016863172.1 |
MRPS18C - mitochondrial ribosomal protein S18C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001297767.1 | 165 | Missense Mutation | GTT,TTT | V,F 7 | NP_001284696.1 | |
NM_001297769.1 | 165 | Missense Mutation | GTT,TTT | V,F 7 | NP_001284698.1 | |
NM_001297770.1 | 165 | Missense Mutation | GTT,TTT | V,F 7 | NP_001284699.1 | |
NM_016067.3 | 165 | Missense Mutation | GTT,TTT | V,F 7 | NP_057151.1 |