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ATGTGAATGGTGTGAGTGGAGACAC[A/T]AAGCCTAACTATATCAGGTGGCAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
|
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Phenotype: |
MIM: 600889 | ||||||||||||||||||||
Literature Links: |
CFHR2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
CFHR2 - complement factor H related 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001312672.1 | Intron | NP_001299601.1 | ||||
NM_005666.3 | Intron | NP_005657.1 | ||||
XM_005245113.3 | Intron | XP_005245170.1 | ||||
XM_011509458.2 | Intron | XP_011507760.1 | ||||
XM_011509459.2 | Intron | XP_011507761.1 | ||||
XM_011509460.2 | Intron | XP_011507762.1 | ||||
XM_017001109.1 | Intron | XP_016856598.1 |