Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCAAGGAATGAATTTATTTTTTGT[A/T]GCATTTCAGGCTTTCCAACCTCATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||
Literature Links: |
SRBD1 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
|
SRBD1 - S1 RNA binding domain 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018079.4 | 2197 | Missense Mutation | CAA,CTA | Q,L 856 | NP_060549.4 | |
XM_011532946.1 | 2197 | Missense Mutation | CAA,CTA | Q,L 840 | XP_011531248.1 | |
XM_017004417.1 | 2197 | Intron | XP_016859906.1 | |||
XM_017004418.1 | 2197 | Missense Mutation | CAA,CTA | Q,L 359 | XP_016859907.1 |