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- SNP ID:
- rs77976555
- Gene
-
CUL7RRP36 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.6: 43037897 - 43037897 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
TCATGGCGTCTCAGCGTGCCCTTGC[C/T]CAGGAGGTGTAGGATGCAGGAGAGG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 609577
MIM: 613475
|
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Literature Links: |
CUL7 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| CUL7 - cullin 7 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001168370.1 | 5264 | Missense Mutation | AGC,GGC | S,G 1714 | NP_001161842.1 | |
| NM_014780.4 | 5264 | Missense Mutation | AGC,GGC | S,G 1630 | NP_055595.2 | |
| XM_005249503.2 | 5264 | Missense Mutation | AGC,GGC | S,G 1682 | XP_005249560.1 | |
| XM_006715285.1 | 5264 | Missense Mutation | AGC,GGC | S,G 1666 | XP_006715348.1 | |
| XM_011515019.2 | 5264 | Missense Mutation | AGC,GGC | S,G 1718 | XP_011513321.1 | |
| XM_011515020.2 | 5264 | Missense Mutation | AGC,GGC | S,G 1686 | XP_011513322.1 | |
| XM_011515021.1 | 5264 | Missense Mutation | AGC,GGC | S,G 921 | XP_011513323.1 | |
| XM_017011533.1 | 5264 | Missense Mutation | AGC,GGC | S,G 1727 | XP_016867022.1 | |
| XM_017011534.1 | 5264 | Missense Mutation | AGC,GGC | S,G 1723 | XP_016867023.1 | |
| XM_017011535.1 | 5264 | Missense Mutation | AGC,GGC | S,G 1695 | XP_016867024.1 | |
| XM_017011536.1 | 5264 | Missense Mutation | AGC,GGC | S,G 1675 | XP_016867025.1 | |
| XM_017011537.1 | 5264 | Missense Mutation | AGC,GGC | S,G 1662 | XP_016867026.1 | |
| XM_017011538.1 | 5264 | Missense Mutation | AGC,GGC | S,G 1643 | XP_016867027.1 | |
| XM_017011539.1 | 5264 | Missense Mutation | AGC,GGC | S,G 1634 | XP_016867028.1 | |
| XM_017011540.1 | 5264 | Intron | XP_016867029.1 | |||
| RRP36 - ribosomal RNA processing 36 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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