Product Details
- SNP ID
-
rs479448
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:7766175 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- GACCAGTCCAAGCAGCAGCAAATCT[A/G]TCAAGAACTGACCGATTTGAAGACT
- Phenotype
-
MIM: 605872
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CLEC4M
PubMed Links
Gene Details
- Gene
- CLEC4M
- Gene Name
- C-type lectin domain family 4 member M
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001144904.1 |
801 |
Missense Mutation |
TAT,TGT |
Y200C |
NP_001138376.1 |
NM_001144905.1 |
801 |
Missense Mutation |
TAT,TGT |
Y227C |
NP_001138377.1 |
NM_001144906.1 |
801 |
Intron |
|
|
NP_001138378.1 |
NM_001144907.1 |
801 |
Intron |
|
|
NP_001138379.1 |
NM_001144908.1 |
801 |
Intron |
|
|
NP_001138380.1 |
NM_001144909.1 |
801 |
Missense Mutation |
TAT,TGT |
Y205C |
NP_001138381.1 |
NM_001144910.1 |
801 |
Missense Mutation |
TAT,TGT |
Y228C |
NP_001138382.1 |
NM_001144911.1 |
801 |
Missense Mutation |
TAT,TGT |
Y223C |
NP_001138383.1 |
NM_014257.4 |
801 |
Missense Mutation |
TAT,TGT |
Y251C |
NP_055072.3 |
XM_006722611.2 |
801 |
Missense Mutation |
TAT,TGT |
Y250C |
XP_006722674.1 |
XM_006722612.3 |
801 |
Missense Mutation |
TAT,TGT |
Y223C |
XP_006722675.1 |
XM_006722613.3 |
801 |
Missense Mutation |
TAT,TGT |
Y223C |
XP_006722676.1 |
XM_006722614.3 |
801 |
Missense Mutation |
TAT,TGT |
Y195C |
XP_006722677.1 |
XM_006722615.2 |
801 |
Missense Mutation |
TAT,TGT |
Y251C |
XP_006722678.1 |
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