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GACAGCCACAGCCGTCAGGGCACCC[C/T]AAGGCCGGGTCAAGAGCTGGCCGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
19 submissions
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Phenotype: |
MIM: 610562 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LINC01137 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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LINC01137 - long intergenic non-protein coding RNA 1137 | ||||||
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There are no transcripts associated with this gene. |
MIR6732 - microRNA 6732 | ||||||
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There are no transcripts associated with this gene. |
ZC3H12A - zinc finger CCCH-type containing 12A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323550.1 | 245 | Missense Mutation | CCA,CTA | P,L 32 | NP_001310479.1 | |
NM_001323551.1 | 245 | UTR 5 | NP_001310480.1 | |||
NM_025079.2 | 245 | Missense Mutation | CCA,CTA | P,L 32 | NP_079355.2 | |
XM_011542198.2 | 245 | Missense Mutation | CCA,CTA | P,L 32 | XP_011540500.1 |