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CCACCCCTGCTTCCCAGGACCTCAC[A/C]TGAGCACTGGTGGTGGCCTGCTCCG
Species: |
Human | |||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 126391 MIM: 603602 | |||||||||||||||||||||||||||||
Literature Links: |
LIG1 PubMed Links | |||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
LIG1 - DNA ligase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000234.2 | 2625 | Silent Mutation | NP_000225.1 | |||
NM_001289063.1 | 2625 | Silent Mutation | NP_001275992.1 | |||
NM_001289064.1 | 2625 | Silent Mutation | NP_001275993.1 | |||
NM_001320970.1 | 2625 | Silent Mutation | NP_001307899.1 | |||
NM_001320971.1 | 2625 | Silent Mutation | NP_001307900.1 | |||
XM_017026809.1 | 2625 | Missense Mutation | XP_016882298.1 |
PLA2G4C - phospholipase A2 group IVC | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |