Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGCTATGAAGTGGACTGGAACCAGA[A/G]CGCCCTCAGCTGTGTAGACCCCCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 602607 | ||||||||||||||||||||
Literature Links: |
SLC22A1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
SLC22A1 - solute carrier family 22 member 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003057.2 | 440 | Missense Mutation | AAC,AGC | N,S 98 | NP_003048.1 | |
NM_153187.1 | 440 | Missense Mutation | AAC,AGC | N,S 98 | NP_694857.1 | |
XM_005267102.4 | 440 | Missense Mutation | AAC,AGC | N,S 98 | XP_005267159.1 | |
XM_005267103.1 | 440 | Missense Mutation | AAC,AGC | N,S 98 | XP_005267160.1 | |
XM_005267104.4 | 440 | Intron | XP_005267161.1 | |||
XM_005267105.4 | 440 | Intron | XP_005267162.1 | |||
XM_006715552.1 | 440 | Missense Mutation | AAC,AGC | N,S 98 | XP_006715615.1 | |
XM_011536074.2 | 440 | Intron | XP_011534376.1 |