Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGAAAGAAGGAAGAAAATAAAAATC[A/C]CTGAAATTATCTATGATCTCACTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 606571 | ||||||||||||||||||||
Literature Links: |
LDLRAD4 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
LDLRAD4 - low density lipoprotein receptor class A domain containing 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001003674.3 | Intron | NP_001003674.1 | ||||
NM_001003675.3 | Intron | NP_001003675.1 | ||||
NM_001276249.1 | Intron | NP_001263178.1 | ||||
NM_001276251.1 | Intron | NP_001263180.1 | ||||
NM_181481.4 | Intron | NP_852146.1 | ||||
NM_181482.4 | Intron | NP_852147.1 | ||||
XM_005258140.1 | Intron | XP_005258197.1 | ||||
XM_006722353.1 | Intron | XP_006722416.1 | ||||
XM_006722354.1 | Intron | XP_006722417.1 | ||||
XM_011525737.1 | Intron | XP_011524039.1 | ||||
XM_011525738.1 | Intron | XP_011524040.1 | ||||
XM_017025961.1 | Intron | XP_016881450.1 | ||||
XM_017025962.1 | Intron | XP_016881451.1 | ||||
XM_017025963.1 | Intron | XP_016881452.1 | ||||
XM_017025964.1 | Intron | XP_016881453.1 | ||||
XM_017025965.1 | Intron | XP_016881454.1 | ||||
XM_017025966.1 | Intron | XP_016881455.1 | ||||
XM_017025967.1 | Intron | XP_016881456.1 | ||||
XM_017025968.1 | Intron | XP_016881457.1 | ||||
XM_017025969.1 | Intron | XP_016881458.1 | ||||
XM_017025970.1 | Intron | XP_016881459.1 | ||||
XM_017025971.1 | Intron | XP_016881460.1 | ||||
XM_017025972.1 | Intron | XP_016881461.1 |