Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGTGGTGGTTCTCACGGGTAGGGC[G/A]TAGCTGCAGGGCCTCCTTGAAGTAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604189 MIM: 607901 MIM: 610470 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
DNAJC4 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)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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DNAJC4 - DnaJ heat shock protein family (Hsp40) member C4 | ||||||
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There are no transcripts associated with this gene. |
FERMT3 - fermitin family member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_031471.5 | 875 | Intron | NP_113659.3 | |||
NM_178443.2 | 875 | Intron | NP_848537.1 | |||
XM_011545294.2 | 875 | Intron | XP_011543596.1 | |||
XM_011545295.2 | 875 | Intron | XP_011543597.1 | |||
XM_017018398.1 | 875 | Intron | XP_016873887.1 | |||
XM_017018399.1 | 875 | Intron | XP_016873888.1 |
NUDT22 - nudix hydrolase 22 | ||||||
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There are no transcripts associated with this gene. |
TRPT1 - tRNA phosphotransferase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033678.3 | 875 | Missense Mutation | CGC,TGC | R,C 221 | NP_001028850.2 | |
NM_001160389.1 | 875 | Missense Mutation | CGC,TGC | R,C 223 | NP_001153861.1 | |
NM_001160390.1 | 875 | Missense Mutation | CGC,TGC | R,C 221 | NP_001153862.1 | |
NM_001160392.1 | 875 | Intron | NP_001153864.1 | |||
NM_001160393.1 | 875 | Missense Mutation | CGC,TGC | R,C 222 | NP_001153865.1 | |
NM_031472.3 | 875 | Missense Mutation | CGC,TGC | R,C 172 | NP_113660.1 | |
XM_005274345.4 | 875 | Missense Mutation | CGC,TGC | R,C 222 | XP_005274402.1 | |
XM_005274346.4 | 875 | Missense Mutation | CGC,TGC | R,C 222 | XP_005274403.1 | |
XM_005274347.4 | 875 | Missense Mutation | CGC,TGC | R,C 173 | XP_005274404.1 | |
XM_006718706.3 | 875 | Missense Mutation | CGC,TGC | R,C 222 | XP_006718769.1 | |
XM_006718707.3 | 875 | Missense Mutation | CGC,TGC | R,C 222 | XP_006718770.1 | |
XM_017018400.1 | 875 | Missense Mutation | CGC,TGC | R,C 173 | XP_016873889.1 | |
XM_017018401.1 | 875 | Intron | XP_016873890.1 |
Set Membership: |
HapMap |