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GCAGAAACAAGAAGAAATCAAAGAG[A/C]ATATAAAGGTATGTGATTGAATAAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602842 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GMNN 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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GMNN - geminin, DNA replication inhibitor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001251989.1 | 174 | Missense Mutation | AAT,CAT | N,H 15 | NP_001238918.1 | |
NM_001251990.1 | 174 | Missense Mutation | AAT,CAT | N,H 15 | NP_001238919.1 | |
NM_001251991.1 | 174 | Missense Mutation | AAT,CAT | N,H 15 | NP_001238920.1 | |
NM_015895.4 | 174 | Missense Mutation | AAT,CAT | N,H 15 | NP_056979.1 | |
XM_005249159.1 | 174 | Missense Mutation | AAT,CAT | N,H 15 | XP_005249216.1 | |
XM_011514651.2 | 174 | Intron | XP_011512953.1 |