Product Details
- SNP ID
-
rs150251718
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.16:71861859 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGTCCTCCGAGTGGATTAAGAGGTG[A/G]CGACCCAATGACCCCGGGGAGCTAA
- Phenotype
-
MIM: 614301
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ATXN1L
PubMed Links
Gene Details
- Gene
- ATXN1L
- Gene Name
- ataxin 1 like
There are no transcripts associated with this gene.
- Gene
- ZNF821
- Gene Name
- zinc finger protein 821
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001201552.1 |
439 |
Silent Mutation |
CGC,CGT |
R167R |
NP_001188481.1 |
| NM_001201553.1 |
439 |
Silent Mutation |
CGC,CGT |
R167R |
NP_001188482.1 |
| NM_001201554.1 |
439 |
Silent Mutation |
CGC,CGT |
R125R |
NP_001188483.1 |
| NM_001201556.1 |
439 |
Intron |
|
|
NP_001188485.1 |
| NM_001318238.1 |
439 |
Silent Mutation |
CGC,CGT |
R17R |
NP_001305167.1 |
| NM_001318239.1 |
439 |
Silent Mutation |
CGC,CGT |
R17R |
NP_001305168.1 |
| NM_017530.2 |
439 |
Silent Mutation |
CGC,CGT |
R125R |
NP_060000.1 |
| XM_005256033.2 |
439 |
Silent Mutation |
CGC,CGT |
R167R |
XP_005256090.1 |
| XM_006721233.1 |
439 |
Silent Mutation |
CGC,CGT |
R167R |
XP_006721296.1 |
| XM_011523211.2 |
439 |
Silent Mutation |
CGC,CGT |
R167R |
XP_011521513.1 |
| XM_011523212.2 |
439 |
Silent Mutation |
CGC,CGT |
R167R |
XP_011521514.1 |
| XM_011523214.2 |
439 |
Silent Mutation |
CGC,CGT |
R17R |
XP_011521516.1 |
| XM_011523215.2 |
439 |
Silent Mutation |
CGC,CGT |
R17R |
XP_011521517.1 |
| XM_011523220.2 |
439 |
Intron |
|
|
XP_011521522.1 |
| XM_017023409.1 |
439 |
Silent Mutation |
CGC,CGT |
R167R |
XP_016878898.1 |
| XM_017023410.1 |
439 |
Silent Mutation |
CGC,CGT |
R167R |
XP_016878899.1 |
| XM_017023411.1 |
439 |
Silent Mutation |
CGC,CGT |
R167R |
XP_016878900.1 |
| XM_017023412.1 |
439 |
Silent Mutation |
CGC,CGT |
R167R |
XP_016878901.1 |
| XM_017023413.1 |
439 |
Silent Mutation |
CGC,CGT |
R157R |
XP_016878902.1 |
| XM_017023414.1 |
439 |
Silent Mutation |
CGC,CGT |
R125R |
XP_016878903.1 |
| XM_017023415.1 |
439 |
Silent Mutation |
CGC,CGT |
R17R |
XP_016878904.1 |
| XM_017023416.1 |
439 |
Silent Mutation |
CGC,CGT |
R17R |
XP_016878905.1 |
| XM_017023417.1 |
439 |
Silent Mutation |
CGC,CGT |
R17R |
XP_016878906.1 |
| XM_017023418.1 |
439 |
Silent Mutation |
CGC,CGT |
R17R |
XP_016878907.1 |
| XM_017023419.1 |
439 |
Silent Mutation |
CGC,CGT |
R17R |
XP_016878908.1 |
| XM_017023420.1 |
439 |
Silent Mutation |
CGC,CGT |
R17R |
XP_016878909.1 |
| XM_017023421.1 |
439 |
Silent Mutation |
CGC,CGT |
R17R |
XP_016878910.1 |
| XM_017023422.1 |
439 |
Silent Mutation |
CGC,CGT |
R17R |
XP_016878911.1 |
| XM_017023423.1 |
439 |
Intron |
|
|
XP_016878912.1 |
| XM_017023424.1 |
439 |
Intron |
|
|
XP_016878913.1 |
| XM_017023425.1 |
439 |
Intron |
|
|
XP_016878914.1 |
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