Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TATGAAGGATTCTGCTTGATTCAAA[C/G]CTTTTATTTTCACCAAAATAAGAAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 189901 MIM: 611832 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GCFC2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
GCFC2 - GC-rich sequence DNA-binding factor 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001201334.1 | 2179 | Missense Mutation | GCT,GGT | A,G 589 | NP_001188263.1 | |
NM_001201335.1 | 2179 | Intron | NP_001188264.1 | |||
NM_003203.4 | 2179 | Missense Mutation | GCT,GGT | A,G 758 | NP_003194.3 | |
XM_005264520.3 | 2179 | Missense Mutation | GCT,GGT | A,G 766 | XP_005264577.1 | |
XM_011533074.2 | 2179 | Missense Mutation | GCT,GGT | A,G 683 | XP_011531376.1 | |
XM_011533075.1 | 2179 | Intron | XP_011531377.1 | |||
XM_017004787.1 | 2179 | Intron | XP_016860276.1 | |||
XM_017004788.1 | 2179 | Intron | XP_016860277.1 |
MRPL19 - mitochondrial ribosomal protein L19 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |