Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGTGCACAATCCAATTCACCTGAAG[C/G]CTCCTGTTTCTGAAGACTTGATGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 142570 MIM: 609433 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HK3 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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HK3 - hexokinase 3 | ||||||
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There are no transcripts associated with this gene. |
UIMC1 - ubiquitin interaction motif containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199297.2 | 1220 | Missense Mutation | GCC,GGC | A,G 648 | NP_001186226.1 | |
NM_001199298.1 | 1220 | Missense Mutation | GCC,GGC | A,G 648 | NP_001186227.1 | |
NM_001317961.1 | 1220 | Missense Mutation | GCC,GGC | A,G 482 | NP_001304890.1 | |
NM_016290.4 | 1220 | Missense Mutation | GCC,GGC | A,G 648 | NP_057374.3 | |
XM_005265930.2 | 1220 | Missense Mutation | GCC,GGC | A,G 648 | XP_005265987.1 | |
XM_005265932.2 | 1220 | Missense Mutation | GCC,GGC | A,G 367 | XP_005265989.1 | |
XM_005265933.2 | 1220 | Missense Mutation | GCC,GGC | A,G 367 | XP_005265990.1 | |
XM_005265934.2 | 1220 | Missense Mutation | GCC,GGC | A,G 345 | XP_005265991.1 | |
XM_005265935.2 | 1220 | Missense Mutation | GCC,GGC | A,G 345 | XP_005265992.1 | |
XM_005265936.2 | 1220 | Missense Mutation | GCC,GGC | A,G 278 | XP_005265993.1 | |
XM_006714871.2 | 1220 | Missense Mutation | GCC,GGC | A,G 648 | XP_006714934.1 | |
XM_006714874.2 | 1220 | Missense Mutation | GCC,GGC | A,G 345 | XP_006714937.1 | |
XM_011534568.2 | 1220 | Intron | XP_011532870.1 | |||
XM_011534570.1 | 1220 | Intron | XP_011532872.1 | |||
XM_017009574.1 | 1220 | Missense Mutation | GCC,GGC | A,G 570 | XP_016865063.1 | |
XM_017009575.1 | 1220 | Missense Mutation | GCC,GGC | A,G 549 | XP_016865064.1 | |
XM_017009576.1 | 1220 | Missense Mutation | GCC,GGC | A,G 367 | XP_016865065.1 | |
XM_017009577.1 | 1220 | Missense Mutation | GCC,GGC | A,G 367 | XP_016865066.1 | |
XM_017009578.1 | 1220 | Missense Mutation | GCC,GGC | A,G 278 | XP_016865067.1 | |
XM_017009579.1 | 1220 | Missense Mutation | GCC,GGC | A,G 278 | XP_016865068.1 |