Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGCCAGGAAGTGAGGGCCCAGCTC[A/G]TCGTAATCAAAACTGCTGAGGAGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 605872 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CLEC4M PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
CLEC4M - C-type lectin domain family 4 member M | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144904.1 | 959 | Missense Mutation | ATC,GTC | I,V 253 | NP_001138376.1 | |
NM_001144905.1 | 959 | Missense Mutation | ATC,GTC | I,V 280 | NP_001138377.1 | |
NM_001144906.1 | 959 | Missense Mutation | ATC,GTC | I,V 168 | NP_001138378.1 | |
NM_001144907.1 | 959 | Missense Mutation | ATC,GTC | I,V 237 | NP_001138379.1 | |
NM_001144908.1 | 959 | Missense Mutation | ATC,GTC | I,V 212 | NP_001138380.1 | |
NM_001144909.1 | 959 | Missense Mutation | ATC,GTC | I,V 258 | NP_001138381.1 | |
NM_001144910.1 | 959 | Missense Mutation | ATC,GTC | I,V 281 | NP_001138382.1 | |
NM_001144911.1 | 959 | Missense Mutation | ATC,GTC | I,V 276 | NP_001138383.1 | |
NM_014257.4 | 959 | Missense Mutation | ATC,GTC | I,V 304 | NP_055072.3 | |
XM_006722611.2 | 959 | Missense Mutation | ATC,GTC | I,V 303 | XP_006722674.1 | |
XM_006722612.3 | 959 | Missense Mutation | ATC,GTC | I,V 276 | XP_006722675.1 | |
XM_006722613.3 | 959 | Missense Mutation | ATC,GTC | I,V 276 | XP_006722676.1 | |
XM_006722614.3 | 959 | Missense Mutation | ATC,GTC | I,V 248 | XP_006722677.1 | |
XM_006722615.2 | 959 | Missense Mutation | ATC,GTC | I,V 304 | XP_006722678.1 |