Product Details
- SNP ID
-
rs77976555
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:43037897 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TCATGGCGTCTCAGCGTGCCCTTGC[C/T]CAGGAGGTGTAGGATGCAGGAGAGG
- Phenotype
-
MIM: 609577
MIM: 613475
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CUL7
PubMed Links
Gene Details
- Gene
- CUL7
- Gene Name
- cullin 7
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001168370.1 |
5264 |
Missense Mutation |
AGC,GGC |
S1714G |
NP_001161842.1 |
NM_014780.4 |
5264 |
Missense Mutation |
AGC,GGC |
S1630G |
NP_055595.2 |
XM_005249503.2 |
5264 |
Missense Mutation |
AGC,GGC |
S1682G |
XP_005249560.1 |
XM_006715285.1 |
5264 |
Missense Mutation |
AGC,GGC |
S1666G |
XP_006715348.1 |
XM_011515019.2 |
5264 |
Missense Mutation |
AGC,GGC |
S1718G |
XP_011513321.1 |
XM_011515020.2 |
5264 |
Missense Mutation |
AGC,GGC |
S1686G |
XP_011513322.1 |
XM_011515021.1 |
5264 |
Missense Mutation |
AGC,GGC |
S921G |
XP_011513323.1 |
XM_017011533.1 |
5264 |
Missense Mutation |
AGC,GGC |
S1727G |
XP_016867022.1 |
XM_017011534.1 |
5264 |
Missense Mutation |
AGC,GGC |
S1723G |
XP_016867023.1 |
XM_017011535.1 |
5264 |
Missense Mutation |
AGC,GGC |
S1695G |
XP_016867024.1 |
XM_017011536.1 |
5264 |
Missense Mutation |
AGC,GGC |
S1675G |
XP_016867025.1 |
XM_017011537.1 |
5264 |
Missense Mutation |
AGC,GGC |
S1662G |
XP_016867026.1 |
XM_017011538.1 |
5264 |
Missense Mutation |
AGC,GGC |
S1643G |
XP_016867027.1 |
XM_017011539.1 |
5264 |
Missense Mutation |
AGC,GGC |
S1634G |
XP_016867028.1 |
XM_017011540.1 |
5264 |
Intron |
|
|
XP_016867029.1 |
- Gene
- RRP36
- Gene Name
- ribosomal RNA processing 36
There are no transcripts associated with this gene.
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