Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGGAGCGGATTTCGAAGTTGCACC[G/T]GTTGAGGATGGCTGACATTCTCTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 602655 MIM: 612762 | ||||||||||||||||||||
Literature Links: |
SLC4A1AP 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 |
SLC4A1AP - solute carrier family 4 member 1 adaptor protein | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018158.2 | 437 | Missense Mutation | CGG,CTG | R,L 52 | NP_060628.2 |
SUPT7L - SPT7-like STAGA complex gamma subunit | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282729.1 | 437 | Intron | NP_001269658.1 | |||
NM_001282730.1 | 437 | Intron | NP_001269659.1 | |||
NM_001282731.1 | 437 | Intron | NP_001269660.1 | |||
NM_001282732.1 | 437 | Intron | NP_001269661.1 | |||
NM_014860.2 | 437 | Intron | NP_055675.1 | |||
XM_005264672.4 | 437 | Intron | XP_005264729.1 |