Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCACAGGCATGGTACCACCAGCCTC[C/G]CCGCTGGTACAGGGCACAGTTACCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609336 MIM: 616808 | ||||||||||||||||||||
Literature Links: |
ANGPTL6 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 |
ANGPTL6 - angiopoietin like 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321411.1 | 1467 | Missense Mutation | CGA,GGA | R,G 416 | NP_001308340.1 | |
NM_031917.2 | 1467 | Missense Mutation | CGA,GGA | R,G 416 | NP_114123.2 | |
XM_005260091.3 | 1467 | Missense Mutation | CGA,GGA | R,G 497 | XP_005260148.1 | |
XM_011528347.2 | 1467 | Missense Mutation | CGA,GGA | R,G 416 | XP_011526649.1 | |
XM_011528348.2 | 1467 | Missense Mutation | CGA,GGA | R,G 483 | XP_011526650.1 | |
XM_011528349.2 | 1467 | Missense Mutation | CGA,GGA | R,G 483 | XP_011526651.1 | |
XM_011528350.2 | 1467 | Missense Mutation | CGA,GGA | R,G 416 | XP_011526652.1 | |
XM_017027347.1 | 1467 | Missense Mutation | CGA,GGA | R,G 416 | XP_016882836.1 |
C19orf66 - chromosome 19 open reading frame 66 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308277.1 | 1467 | UTR 3 | NP_001295206.1 | |||
NM_018381.3 | 1467 | UTR 3 | NP_060851.2 | |||
XM_011528121.1 | 1467 | UTR 3 | XP_011526423.1 | |||
XM_011528122.1 | 1467 | Intron | XP_011526424.1 | |||
XM_017026934.1 | 1467 | UTR 3 | XP_016882423.1 |