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GACCCTTCCTTTTCTTCTAGATCCA[A/G]TCTAAGTTGGTTGGTAATTTCTTTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610242 MIM: 610241 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C7orf13 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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C7orf13 - chromosome 7 open reading frame 13 | ||||||
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There are no transcripts associated with this gene. |
RNF32 - ring finger protein 32 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184996.1 | Intron | NP_001171925.1 | ||||
NM_001184997.1 | Intron | NP_001171926.1 | ||||
NM_001308273.1 | Intron | NP_001295202.1 | ||||
NM_001308274.1 | Intron | NP_001295203.1 | ||||
NM_030936.3 | Intron | NP_112198.1 |