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TGTCATCCTGTGTACTCTGCTCACT[C/T]GTTGCTGTTTCTGTTGTTGCTGCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613946 MIM: 602878 MIM: 606474 | ||||||||||||||||||||
Literature Links: |
DNAJC5G PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
DNAJC5G - DnaJ heat shock protein family (Hsp40) member C5 gamma | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303127.1 | 762 | Missense Mutation | CGT,TGT | R,C 136 | NP_001290056.1 | |
NM_001303128.1 | 762 | Silent Mutation | CTC,CTT | L,L 48 | NP_001290057.1 | |
NM_173650.2 | 762 | Missense Mutation | CGT,TGT | R,C 136 | NP_775921.1 | |
XM_006711995.3 | 762 | Missense Mutation | CGT,TGT | R,C 136 | XP_006712058.1 | |
XM_017003872.1 | 762 | Missense Mutation | CGT,TGT | R,C 136 | XP_016859361.1 | |
XM_017003873.1 | 762 | Missense Mutation | CGT,TGT | R,C 136 | XP_016859362.1 | |
XM_017003874.1 | 762 | Missense Mutation | CGT,TGT | R,C 136 | XP_016859363.1 |
SLC30A3 - solute carrier family 30 member 3 | ||||||
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There are no transcripts associated with this gene. |
TRIM54 - tripartite motif containing 54 | ||||||
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There are no transcripts associated with this gene. |