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Search Thermo Fisher Scientific
GAGCCGCTTGGCCTCTCGCTCTCGG[A/C]TGAGCCGGGCCTGCCGCTTTTCCGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614301 | ||||||||||||||||||||
Literature Links: |
ATXN1L 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 |
ATXN1L - ataxin 1 like | ||||||
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There are no transcripts associated with this gene. |
ZNF821 - zinc finger protein 821 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001201552.1 | 969 | Missense Mutation | AGC,ATC | S,I 344 | NP_001188481.1 | |
NM_001201553.1 | 969 | Missense Mutation | AGC,ATC | S,I 344 | NP_001188482.1 | |
NM_001201554.1 | 969 | Missense Mutation | AGC,ATC | S,I 302 | NP_001188483.1 | |
NM_001201556.1 | 969 | UTR 3 | NP_001188485.1 | |||
NM_001318238.1 | 969 | Missense Mutation | AGC,ATC | S,I 194 | NP_001305167.1 | |
NM_001318239.1 | 969 | Missense Mutation | AGC,ATC | S,I 194 | NP_001305168.1 | |
NM_017530.2 | 969 | Missense Mutation | AGC,ATC | S,I 302 | NP_060000.1 | |
XM_005256033.2 | 969 | Missense Mutation | AGC,ATC | S,I 344 | XP_005256090.1 | |
XM_006721233.1 | 969 | Missense Mutation | AGC,ATC | S,I 344 | XP_006721296.1 | |
XM_011523211.2 | 969 | Missense Mutation | AGC,ATC | S,I 344 | XP_011521513.1 | |
XM_011523212.2 | 969 | Missense Mutation | AGC,ATC | S,I 344 | XP_011521514.1 | |
XM_011523214.2 | 969 | Missense Mutation | AGC,ATC | S,I 194 | XP_011521516.1 | |
XM_011523215.2 | 969 | Missense Mutation | AGC,ATC | S,I 194 | XP_011521517.1 | |
XM_011523220.2 | 969 | Missense Mutation | AGC,ATC | S,I 141 | XP_011521522.1 | |
XM_017023409.1 | 969 | Missense Mutation | AGC,ATC | S,I 344 | XP_016878898.1 | |
XM_017023410.1 | 969 | Missense Mutation | AGC,ATC | S,I 344 | XP_016878899.1 | |
XM_017023411.1 | 969 | Missense Mutation | AGC,ATC | S,I 344 | XP_016878900.1 | |
XM_017023412.1 | 969 | Missense Mutation | AGC,ATC | S,I 344 | XP_016878901.1 | |
XM_017023413.1 | 969 | Missense Mutation | AGC,ATC | S,I 334 | XP_016878902.1 | |
XM_017023414.1 | 969 | Missense Mutation | AGC,ATC | S,I 302 | XP_016878903.1 | |
XM_017023415.1 | 969 | Missense Mutation | AGC,ATC | S,I 194 | XP_016878904.1 | |
XM_017023416.1 | 969 | Missense Mutation | AGC,ATC | S,I 194 | XP_016878905.1 | |
XM_017023417.1 | 969 | Missense Mutation | AGC,ATC | S,I 194 | XP_016878906.1 | |
XM_017023418.1 | 969 | Missense Mutation | AGC,ATC | S,I 194 | XP_016878907.1 | |
XM_017023419.1 | 969 | Missense Mutation | AGC,ATC | S,I 194 | XP_016878908.1 | |
XM_017023420.1 | 969 | Missense Mutation | AGC,ATC | S,I 194 | XP_016878909.1 | |
XM_017023421.1 | 969 | Missense Mutation | AGC,ATC | S,I 194 | XP_016878910.1 | |
XM_017023422.1 | 969 | Missense Mutation | AGC,ATC | S,I 194 | XP_016878911.1 | |
XM_017023423.1 | 969 | Missense Mutation | AGC,ATC | S,I 141 | XP_016878912.1 | |
XM_017023424.1 | 969 | Missense Mutation | AGC,ATC | S,I 141 | XP_016878913.1 | |
XM_017023425.1 | 969 | Missense Mutation | AGC,ATC | S,I 141 | XP_016878914.1 |