Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGCAGCACTTGAAGGAGGCCTCCAC[A/G]GCACCCACGGCGGTGGCTTCTGTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 179050 | ||||||||||||||||||||
Literature Links: |
GRAMD2 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 |
GRAMD2 - GRAM domain containing 2 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
PKM - pyruvate kinase, muscle | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001206796.2 | 1556 | Intron | NP_001193725.1 | |||
NM_001206797.2 | 1556 | Silent Mutation | GCC,GCT | A,A 342 | NP_001193726.1 | |
NM_001206798.2 | 1556 | Silent Mutation | GCC,GCT | A,A 401 | NP_001193727.1 | |
NM_001206799.1 | 1556 | Intron | NP_001193728.1 | |||
NM_001316318.1 | 1556 | Intron | NP_001303247.1 | |||
NM_002654.5 | 1556 | Silent Mutation | GCC,GCT | A,A 416 | NP_002645.3 | |
NM_182470.3 | 1556 | Intron | NP_872270.1 | |||
NM_182471.3 | 1556 | Intron | NP_872271.1 | |||
XM_005254443.1 | 1556 | Silent Mutation | GCC,GCT | A,A 476 | XP_005254500.1 | |
XM_005254445.4 | 1556 | Intron | XP_005254502.1 | |||
XM_006720570.1 | 1556 | Silent Mutation | GCC,GCT | A,A 490 | XP_006720633.1 | |
XM_011521670.2 | 1556 | Silent Mutation | GCC,GCT | A,A 451 | XP_011519972.1 | |
XM_017022313.1 | 1556 | Intron | XP_016877802.1 |