Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGTTGGGGAGTCTGGCTGGTTCCAG[-/C]AAGCAAGCCTTCCTCATCTTATGCC
Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 602607 | ||||||||||||||||||||||||||||||||
Literature Links: |
SLC22A1 PubMed Links | ||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global - Not Available | Caucasian
|
CEPH (CEU) - Not Available | |||
EAS - Not Available | African American
|
YRI (Yoruba) - Not Available | |||
SAS - Not Available | Japanese
|
CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Chinese
|
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 | 201 | Frame Shift InDel | CAC,CAG | H,Q 18 | NP_003048.1 | |
NM_153187.1 | 201 | Frame Shift InDel | CAC,CAG | H,Q 18 | NP_694857.1 | |
XM_005267102.4 | 201 | Frame Shift InDel | CAC,CAG | H,Q 18 | XP_005267159.1 | |
XM_005267103.1 | 201 | Frame Shift InDel | CAC,CAG | H,Q 18 | XP_005267160.1 | |
XM_005267104.4 | 201 | Intron | XP_005267161.1 | |||
XM_005267105.4 | 201 | Intron | XP_005267162.1 | |||
XM_006715552.1 | 201 | Frame Shift InDel | CAC,CAG | H,Q 18 | XP_006715615.1 | |
XM_011536074.2 | 201 | Intron | XP_011534376.1 |
Set Membership: |
DME Validated Inventoried |