Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 606610 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NSFL1C 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
|
NSFL1C - NSFL1 cofactor | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
SIRPB2 - signal regulatory protein beta 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001122962.1 | 569 | Intron | NP_001116434.1 | |||
NM_001134836.1 | 569 | Intron | NP_001128308.1 | |||
XM_005260708.4 | 569 | Missense Mutation | GGA,GTA | G,V 311 | XP_005260765.1 | |
XM_005260709.3 | 569 | Missense Mutation | GGA,GTA | G,V 213 | XP_005260766.1 | |
XM_011529221.2 | 569 | Missense Mutation | GGA,GTA | G,V 264 | XP_011527523.1 | |
XM_011529223.2 | 569 | Missense Mutation | GGA,GTA | G,V 173 | XP_011527525.1 | |
XM_011529224.2 | 569 | Missense Mutation | GGA,GTA | G,V 173 | XP_011527526.1 | |
XM_011529225.2 | 569 | Missense Mutation | GGA,GTA | G,V 164 | XP_011527527.1 |