Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCGTTTTCCACCTGTGACTACTGGC[C/T]GTGCATATTCTACAAAATCATCTAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610620 | ||||||||||||||||||||
Literature Links: |
ADPRHL1 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 |
ADPRHL1 - ADP-ribosylhydrolase like 1 | ||||||
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There are no transcripts associated with this gene. |
DCUN1D2 - defective in cullin neddylation 1 domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001014283.1 | 4705 | Missense Mutation | NP_001014305.1 | |||
XM_017020643.1 | 4705 | Missense Mutation | XP_016876132.1 | |||
XM_017020644.1 | 4705 | Missense Mutation | XP_016876133.1 | |||
XM_017020645.1 | 4705 | Missense Mutation | XP_016876134.1 | |||
XM_017020646.1 | 4705 | Missense Mutation | XP_016876135.1 | |||
XM_017020647.1 | 4705 | Missense Mutation | XP_016876136.1 | |||
XM_017020648.1 | 4705 | Missense Mutation | XP_016876137.1 | |||
XM_017020649.1 | 4705 | Missense Mutation | XP_016876138.1 |