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AAGTGGAATTTTGTGGTTACACTAC[A/G]ACCCATCCTTCAGAGAGCAAAATTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609733 MIM: 613715 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LNX2 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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LNX2 - ligand of numb-protein X 2 | ||||||
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There are no transcripts associated with this gene. |
POLR1D - RNA polymerase I subunit D | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001206559.1 | 1261 | Intron | NP_001193488.1 | |||
NM_015972.3 | 1261 | Silent Mutation | ACA,ACG | T,T 72 | NP_057056.1 | |
NM_152705.2 | 1261 | Intron | NP_689918.1 | |||
XM_005266412.1 | 1261 | Silent Mutation | ACA,ACG | T,T 72 | XP_005266469.1 | |
XM_005266414.2 | 1261 | Intron | XP_005266471.1 | |||
XM_017020622.1 | 1261 | Intron | XP_016876111.1 | |||
XM_017020623.1 | 1261 | Intron | XP_016876112.1 |