Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTGCCATCCACCCATTTCCAAGAGC[C/G]ATCACTGTCCGTGAGACCTATCCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 108361 | ||||||||||||||||||||
Literature Links: |
ASGR2 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 |
ASGR2 - asialoglycoprotein receptor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001181.4 | 951 | Missense Mutation | CGC,GGC | R,G 242 | NP_001172.1 | |
NM_001201352.1 | 951 | Missense Mutation | CGC,GGC | R,G 237 | NP_001188281.1 | |
NM_080912.3 | 951 | Missense Mutation | CGC,GGC | R,G 242 | NP_550434.1 | |
NM_080913.3 | 951 | Missense Mutation | CGC,GGC | R,G 218 | NP_550435.1 | |
NM_080914.2 | 951 | Missense Mutation | CGC,GGC | R,G 223 | NP_550436.1 | |
XM_005256648.2 | 951 | Missense Mutation | CGC,GGC | R,G 218 | XP_005256705.1 | |
XM_006721524.2 | 951 | Missense Mutation | CGC,GGC | R,G 179 | XP_006721587.2 | |
XM_006721526.1 | 951 | Missense Mutation | CGC,GGC | R,G 218 | XP_006721589.1 | |
XM_011523862.2 | 951 | Missense Mutation | CGC,GGC | R,G 341 | XP_011522164.2 | |
XM_011523863.2 | 951 | Missense Mutation | CGC,GGC | R,G 230 | XP_011522165.1 | |
XM_011523864.2 | 951 | Missense Mutation | CGC,GGC | R,G 249 | XP_011522166.1 | |
XM_011523865.1 | 951 | Missense Mutation | CGC,GGC | R,G 230 | XP_011522167.1 | |
XM_011523866.1 | 951 | Missense Mutation | CGC,GGC | R,G 230 | XP_011522168.1 | |
XM_017024651.1 | 951 | Missense Mutation | CGC,GGC | R,G 223 | XP_016880140.1 | |
XM_017024652.1 | 951 | Missense Mutation | CGC,GGC | R,G 242 | XP_016880141.1 | |
XM_017024653.1 | 951 | Missense Mutation | CGC,GGC | R,G 242 | XP_016880142.1 |