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AACTTTGTCCCCAGCAGGGAGCAAG[G/T]CTGGGGACTCCTGGCAGTGGCGGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 612738 | ||||||||||||||||||||
Literature Links: |
SLC9C1 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 |
SLC9C1 - solute carrier family 9 member C1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320531.1 | 3524 | Missense Mutation | NP_001307460.1 | |||
NM_183061.2 | 3524 | Missense Mutation | NP_898884.1 | |||
XM_006713603.2 | 3524 | Missense Mutation | XP_006713666.1 | |||
XM_011512718.1 | 3524 | Missense Mutation | XP_011511020.1 | |||
XM_011512719.1 | 3524 | Missense Mutation | XP_011511021.1 | |||
XM_011512720.1 | 3524 | Missense Mutation | XP_011511022.1 | |||
XM_011512721.1 | 3524 | Missense Mutation | XP_011511023.1 | |||
XM_011512724.1 | 3524 | Intron | XP_011511026.1 | |||
XM_011512725.2 | 3524 | Missense Mutation | XP_011511027.1 | |||
XM_011512726.2 | 3524 | Intron | XP_011511028.1 | |||
XM_011512727.2 | 3524 | Intron | XP_011511029.1 | |||
XM_017006246.1 | 3524 | Missense Mutation | XP_016861735.1 | |||
XM_017006247.1 | 3524 | Missense Mutation | XP_016861736.1 | |||
XM_017006248.1 | 3524 | Missense Mutation | XP_016861737.1 | |||
XM_017006249.1 | 3524 | Intron | XP_016861738.1 | |||
XM_017006250.1 | 3524 | Intron | XP_016861739.1 |