Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTCCCTCTGGGCTATAGCACACAGG[A/G]CCACAGCGCAACTGGGGCTCTTCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 608294 | ||||||||||||||||||||
Literature Links: |
FCF1P2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | 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 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
NME6 - NME/NM23 nucleoside diphosphate kinase 6 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308426.1 | 832 | Silent Mutation | GGC,GGT | G,G 164 | NP_001295355.1 | |
NM_001308427.1 | 832 | Silent Mutation | GGC,GGT | G,G 164 | NP_001295356.1 | |
NM_001308428.1 | 832 | Silent Mutation | GGC,GGT | G,G 164 | NP_001295357.1 | |
NM_001308430.1 | 832 | Missense Mutation | GCC,GTC | A,V 159 | NP_001295359.1 | |
NM_001308431.1 | 832 | Missense Mutation | GCC,GTC | A,V 151 | NP_001295360.1 | |
NM_001308433.1 | 832 | Missense Mutation | GCC,GTC | A,V 151 | NP_001295362.1 | |
NM_001308434.1 | 832 | Silent Mutation | GGC,GGT | G,G 119 | NP_001295363.1 | |
NM_001308435.1 | 832 | Silent Mutation | GGC,GGT | G,G 97 | NP_001295364.1 | |
NM_005793.4 | 832 | Silent Mutation | GGC,GGT | G,G 172 | NP_005784.1 | |
XM_017005511.1 | 832 | Intron | XP_016861000.1 | |||
XM_017005512.1 | 832 | Intron | XP_016861001.1 | |||
XM_017005513.1 | 832 | Silent Mutation | GGC,GGT | G,G 168 | XP_016861002.1 | |
XM_017005514.1 | 832 | Silent Mutation | GGC,GGT | G,G 164 | XP_016861003.1 | |
XM_017005515.1 | 832 | Missense Mutation | GCC,GTC | A,V 151 | XP_016861004.1 | |
XM_017005516.1 | 832 | Intron | XP_016861005.1 | |||
XM_017005517.1 | 832 | Silent Mutation | GGC,GGT | G,G 92 | XP_016861006.1 | |
XM_017005518.1 | 832 | Silent Mutation | GGC,GGT | G,G 89 | XP_016861007.1 |