Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 603095 MIM: 180473 MIM: 603443 MIM: 611440 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
B3GALT4 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
|
B3GALT4 - beta-1,3-galactosyltransferase 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003782.3 | 1789 | Intron | NP_003773.1 |
MIR6873 - microRNA 6873 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
RPS18 - ribosomal protein S18 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
VPS52 - VPS52, GARP complex subunit | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
WDR46 - WD repeat domain 46 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164267.1 | 1789 | Missense Mutation | ACG,ATG | T,M 519 | NP_001157739.1 | |
NM_005452.5 | 1789 | Missense Mutation | ACG,ATG | T,M 573 | NP_005443.3 | |
XM_017011484.1 | 1789 | Missense Mutation | ACG,ATG | T,M 573 | XP_016866973.1 | |
XM_017011485.1 | 1789 | Missense Mutation | ACG,ATG | T,M 251 | XP_016866974.1 | |
XM_017011486.1 | 1789 | Missense Mutation | ACG,ATG | T,M 229 | XP_016866975.1 | |
XM_017011487.1 | 1789 | Missense Mutation | ACG,ATG | T,M 229 | XP_016866976.1 |