Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTAGTGATGCATTAGGTAACTGGAA[C/T]AACTATGCCACAATCTGTCCATTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||
Literature Links: |
C19orf47 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
|
C19orf47 - chromosome 19 open reading frame 47 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256440.1 | Intron | NP_001243369.1 | ||||
NM_001256441.1 | Intron | NP_001243370.1 | ||||
XM_005258520.2 | Intron | XP_005258577.1 | ||||
XM_011526460.2 | Intron | XP_011524762.1 | ||||
XM_017026291.1 | Intron | XP_016881780.1 | ||||
XM_017026292.1 | Intron | XP_016881781.1 | ||||
XM_017026293.1 | Intron | XP_016881782.1 | ||||
XM_017026294.1 | Intron | XP_016881783.1 | ||||
XM_017026295.1 | Intron | XP_016881784.1 |