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AGGGCCAGAGCGATGGAGGCATCCA[C/T]CTGGCAGAAGGCAAACTCTGCAAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611800 MIM: 612053 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LINC01126 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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LINC01126 - long intergenic non-protein coding RNA 1126 | ||||||
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There are no transcripts associated with this gene. |
THADA - THADA, armadillo repeat containing | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001083953.1 | 5666 | Missense Mutation | ATG,GTG | M,V 1772 | NP_001077422.1 | |
NM_001271643.1 | 5666 | Intron | NP_001258572.1 | |||
NM_001271644.1 | 5666 | Intron | NP_001258573.1 | |||
NM_022065.4 | 5666 | Missense Mutation | ATG,GTG | M,V 1772 | NP_071348.3 | |
XM_006712061.3 | 5666 | Missense Mutation | ATG,GTG | M,V 1772 | XP_006712124.1 | |
XM_006712062.1 | 5666 | Missense Mutation | ATG,GTG | M,V 1771 | XP_006712125.1 | |
XM_006712063.1 | 5666 | Missense Mutation | ATG,GTG | M,V 1732 | XP_006712126.1 | |
XM_006712064.2 | 5666 | Missense Mutation | ATG,GTG | M,V 1728 | XP_006712127.1 | |
XM_006712065.1 | 5666 | Missense Mutation | ATG,GTG | M,V 1698 | XP_006712128.1 | |
XM_006712066.1 | 5666 | Missense Mutation | ATG,GTG | M,V 1651 | XP_006712129.1 | |
XM_006712067.1 | 5666 | Missense Mutation | ATG,GTG | M,V 1650 | XP_006712130.1 | |
XM_006712068.3 | 5666 | Intron | XP_006712131.1 | |||
XM_006712069.3 | 5666 | Missense Mutation | ATG,GTG | M,V 955 | XP_006712132.1 | |
XM_011533015.2 | 5666 | Intron | XP_011531317.1 | |||
XM_017004674.1 | 5666 | Missense Mutation | ATG,GTG | M,V 1731 | XP_016860163.1 | |
XM_017004675.1 | 5666 | Missense Mutation | ATG,GTG | M,V 876 | XP_016860164.1 |
ZFP36L2 - ZFP36 ring finger protein like 2 | ||||||
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There are no transcripts associated with this gene. |