Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATCACTACCAGACGGTGTCCGAAAC[A/G]ATTGCTCAGGACTGTGGCGAGGGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610008 MIM: 603880 | ||||||||||||||||||||
Literature Links: |
ARSG PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
SLC16A6 - solute carrier family 16 member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001174166.1 | 572 | Missense Mutation | CGT,TGT | R,C 87 | NP_001167637.1 | |
NM_004694.4 | 572 | Missense Mutation | CGT,TGT | R,C 87 | NP_004685.2 | |
XM_005257789.3 | 572 | Missense Mutation | CGT,TGT | R,C 91 | XP_005257846.2 | |
XM_011525461.2 | 572 | Missense Mutation | CGT,TGT | R,C 87 | XP_011523763.1 | |
XM_017025291.1 | 572 | Missense Mutation | CGT,TGT | R,C 87 | XP_016880780.1 | |
XM_017025292.1 | 572 | Missense Mutation | CGT,TGT | R,C 87 | XP_016880781.1 |