Product Details
- SNP ID
-
rs201866305
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:157150315 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTCTAGCTGCAAGGTAGATGCAAGC[A/G]CATGCTATAGTCTCTGGTTGAAATC
- Phenotype
-
MIM: 613384
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CCNL1
PubMed Links
Gene Details
- Gene
- CCNL1
- Gene Name
- cyclin L1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001308185.1 |
878 |
Silent Mutation |
TGC,TGT |
C247C |
NP_001295114.1 |
| NM_020307.3 |
878 |
Silent Mutation |
TGC,TGT |
C247C |
NP_064703.1 |
| XM_005247648.3 |
878 |
Silent Mutation |
TGC,TGT |
C92C |
XP_005247705.1 |
| XM_006713710.3 |
878 |
Silent Mutation |
TGC,TGT |
C247C |
XP_006713773.1 |
| XM_011513011.2 |
878 |
Silent Mutation |
TGC,TGT |
C92C |
XP_011511313.1 |
| XM_017006891.1 |
878 |
Silent Mutation |
TGC,TGT |
C41C |
XP_016862380.1 |
| XM_017006892.1 |
878 |
Silent Mutation |
TGC,TGT |
C20C |
XP_016862381.1 |
| XM_017006893.1 |
878 |
Silent Mutation |
TGC,TGT |
C20C |
XP_016862382.1 |
| XM_017006894.1 |
878 |
Silent Mutation |
TGC,TGT |
C20C |
XP_016862383.1 |
| XM_017006895.1 |
878 |
Silent Mutation |
TGC,TGT |
C20C |
XP_016862384.1 |
| XM_017006896.1 |
878 |
Silent Mutation |
TGC,TGT |
C20C |
XP_016862385.1 |
| XM_017006897.1 |
878 |
Silent Mutation |
TGC,TGT |
C41C |
XP_016862386.1 |
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