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ACAGGTGGTGCGCGTGGGCAGGGCG[C/T]GGGGACATGGGGCCCGACATGGAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607712 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HIC2 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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HIC2 - hypermethylated in cancer 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015094.2 | 181 | Silent Mutation | CGC,CGT | R,R 16 | NP_055909.2 | |
XM_011530007.2 | 181 | Silent Mutation | CGC,CGT | R,R 16 | XP_011528309.1 | |
XM_011530008.2 | 181 | Silent Mutation | CGC,CGT | R,R 16 | XP_011528310.1 | |
XM_011530009.2 | 181 | Silent Mutation | CGC,CGT | R,R 16 | XP_011528311.1 | |
XM_011530010.2 | 181 | Silent Mutation | CGC,CGT | R,R 16 | XP_011528312.1 | |
XM_017028669.1 | 181 | UTR 5 | XP_016884158.1 |