Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CACCCCTAAGGCTCCCAACCTGGAG[C/T]CTCCACTCCCAGAAGAGGAAAAGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
12 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 |
---|---|---|
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 |
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 | 517 | Missense Mutation | CCT,TCT | P,S 123 | NP_001310479.1 | |
NM_001323551.1 | 517 | UTR 5 | NP_001310480.1 | |||
NM_025079.2 | 517 | Missense Mutation | CCT,TCT | P,S 123 | NP_079355.2 | |
XM_011542198.2 | 517 | Missense Mutation | CCT,TCT | P,S 123 | XP_011540500.1 |