Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCACACACCTGAGGGAATCCCTGGG[G/A]CTTTGAACTCAAGGAAGGGCACCCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 171150 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SULT1A1 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian
|
CEPH (CEU) - Not Available | ||||||
EAS
|
African American
|
YRI (Yoruba) - Not Available | ||||||
SAS
|
Japanese
|
CHB (Han Chinese) - Not Available | ||||||
AFR
|
Chinese
|
JPT (Japanese) - Not Available | ||||||
EUR
|
||||||||
AMR
|
SULT1A1 - sulfotransferase family 1A member 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001055.3 | 687 | Missense Mutation | NP_001046.2 | |||
NM_177529.2 | 687 | Missense Mutation | NP_803565.1 | |||
NM_177530.2 | 687 | Missense Mutation | NP_803566.1 | |||
NM_177534.2 | 687 | Missense Mutation | NP_803878.1 | |||
NM_177536.3 | 687 | Intron | NP_803880.1 | |||
XM_017023604.1 | 687 | Missense Mutation | XP_016879093.1 | |||
XM_017023605.1 | 687 | Missense Mutation | XP_016879094.1 | |||
XM_017023606.1 | 687 | Missense Mutation | XP_016879095.1 | |||
XM_017023607.1 | 687 | Missense Mutation | XP_016879096.1 | |||
XM_017023608.1 | 687 | Missense Mutation | XP_016879097.1 | |||
XM_017023609.1 | 687 | Missense Mutation | XP_016879098.1 | |||
XM_017023610.1 | 687 | Missense Mutation | XP_016879099.1 | |||
XM_017023611.1 | 687 | Missense Mutation | XP_016879100.1 | |||
XM_017023612.1 | 687 | Missense Mutation | XP_016879101.1 | |||
XM_017023613.1 | 687 | Missense Mutation | XP_016879102.1 |
Set Membership: |
DME Validated Inventoried |