Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGCCTGGGCTGGGACCTTAGCCTTT[A/G]TCCTGTTCCTCTTCTTCCTGCCCAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 604885 MIM: 612584 | ||||||||||||||||||||
Literature Links: |
MYBBP1A 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 |
MYBBP1A - MYB binding protein 1a | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001105538.1 | 3709 | Missense Mutation | ACA,ATA | T,I 1216 | NP_001099008.1 | |
NM_014520.3 | 3709 | Missense Mutation | ACA,ATA | T,I 1216 | NP_055335.2 | |
XM_011523616.2 | 3709 | Missense Mutation | ACA,ATA | T,I 964 | XP_011521918.1 |
SPNS2 - sphingolipid transporter 2 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |