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CCTTTCCGAAGAGAAGCTGGCCCTC[A/G]ACAACAATGCCAGCGCTAGTGGCAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610734 MIM: 613597 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ANKRD2 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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ANKRD2 - ankyrin repeat domain 2 | ||||||
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There are no transcripts associated with this gene. |
C10orf62 - chromosome 10 open reading frame 62 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001009997.2 | 353 | Missense Mutation | AAC,GAC | N,D 50 | NP_001009997.2 |
HOGA1 - 4-hydroxy-2-oxoglutarate aldolase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001134670.1 | 353 | Intron | NP_001128142.1 | |||
NM_138413.3 | 353 | Intron | NP_612422.2 |