Product Details
- SNP ID
-
rs141709966
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:7101622 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTCCGCCTTTTCTCACACACCCAGC[A/G]GTACACCTGCAGGCAGAAGTCATCG
- Phenotype
-
MIM: 108361
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ASGR2
PubMed Links
Gene Details
- Gene
- ASGR2
- Gene Name
- asialoglycoprotein receptor 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001181.4 |
1116 |
Missense Mutation |
CGC,TGC |
R297C |
NP_001172.1 |
NM_001201352.1 |
1116 |
Missense Mutation |
CGC,TGC |
R292C |
NP_001188281.1 |
NM_080912.3 |
1116 |
Missense Mutation |
CGC,TGC |
R297C |
NP_550434.1 |
NM_080913.3 |
1116 |
Missense Mutation |
CGC,TGC |
R273C |
NP_550435.1 |
NM_080914.2 |
1116 |
Missense Mutation |
CGC,TGC |
R278C |
NP_550436.1 |
XM_005256648.2 |
1116 |
Missense Mutation |
CGC,TGC |
R273C |
XP_005256705.1 |
XM_006721524.2 |
1116 |
Missense Mutation |
CGC,TGC |
R234C |
XP_006721587.2 |
XM_006721526.1 |
1116 |
Missense Mutation |
CGC,TGC |
R273C |
XP_006721589.1 |
XM_011523862.2 |
1116 |
Missense Mutation |
CGC,TGC |
R396C |
XP_011522164.2 |
XM_011523863.2 |
1116 |
Missense Mutation |
CGC,TGC |
R285C |
XP_011522165.1 |
XM_011523864.2 |
1116 |
Missense Mutation |
CGC,TGC |
R304C |
XP_011522166.1 |
XM_011523865.1 |
1116 |
Missense Mutation |
CGC,TGC |
R285C |
XP_011522167.1 |
XM_011523866.1 |
1116 |
Missense Mutation |
CGC,TGC |
R285C |
XP_011522168.1 |
XM_017024651.1 |
1116 |
Missense Mutation |
CGC,TGC |
R278C |
XP_016880140.1 |
XM_017024652.1 |
1116 |
Missense Mutation |
CGC,TGC |
R297C |
XP_016880141.1 |
XM_017024653.1 |
1116 |
Missense Mutation |
CGC,TGC |
R297C |
XP_016880142.1 |
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