Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTCCTCTGTGTCCTTATTCCACTT[C/T]CTCTGCAGCCCTCCAGGGGACCCCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 606470 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NHP2 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
|
NHP2 - NHP2 ribonucleoprotein | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
RMND5B - required for meiotic nuclear division 5 homolog B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288794.1 | Intron | NP_001275723.1 | ||||
NM_001288795.1 | Intron | NP_001275724.1 | ||||
NM_022762.4 | Intron | NP_073599.2 | ||||
XM_005265969.3 | Intron | XP_005266026.1 | ||||
XM_005265971.4 | Intron | XP_005266028.1 | ||||
XM_005265972.3 | Intron | XP_005266029.1 | ||||
XM_017009727.1 | Intron | XP_016865216.1 | ||||
XM_017009728.1 | Intron | XP_016865217.1 |