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TTCACTGAAGTCAGGGAAGAAGGCT[G/T]CAATCTCTCTGCTGGCTGAAACCAC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 608294 | |||||||||||||||||||||||
Literature Links: |
FCF1P2 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
FCF1P2 - FCF1 pseudogene 2 | ||||||
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There are no transcripts associated with this gene. |
NME6 - NME/NM23 nucleoside diphosphate kinase 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308426.1 | 765 | Missense Mutation | GAA,GCA | E,A 142 | NP_001295355.1 | |
NM_001308427.1 | 765 | Missense Mutation | GAA,GCA | E,A 142 | NP_001295356.1 | |
NM_001308428.1 | 765 | Missense Mutation | GAA,GCA | E,A 142 | NP_001295357.1 | |
NM_001308430.1 | 765 | Missense Mutation | AAG,CAG | K,Q 137 | NP_001295359.1 | |
NM_001308431.1 | 765 | Missense Mutation | AAG,CAG | K,Q 129 | NP_001295360.1 | |
NM_001308433.1 | 765 | Missense Mutation | AAG,CAG | K,Q 129 | NP_001295362.1 | |
NM_001308434.1 | 765 | Missense Mutation | GAA,GCA | E,A 97 | NP_001295363.1 | |
NM_001308435.1 | 765 | Missense Mutation | GAA,GCA | E,A 75 | NP_001295364.1 | |
NM_005793.4 | 765 | Missense Mutation | GAA,GCA | E,A 150 | NP_005784.1 | |
XM_017005511.1 | 765 | Intron | XP_016861000.1 | |||
XM_017005512.1 | 765 | Intron | XP_016861001.1 | |||
XM_017005513.1 | 765 | Missense Mutation | GAA,GCA | E,A 146 | XP_016861002.1 | |
XM_017005514.1 | 765 | Missense Mutation | GAA,GCA | E,A 142 | XP_016861003.1 | |
XM_017005515.1 | 765 | Missense Mutation | AAG,CAG | K,Q 129 | XP_016861004.1 | |
XM_017005516.1 | 765 | Intron | XP_016861005.1 | |||
XM_017005517.1 | 765 | Missense Mutation | GAA,GCA | E,A 70 | XP_016861006.1 | |
XM_017005518.1 | 765 | Missense Mutation | GAA,GCA | E,A 67 | XP_016861007.1 |