Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTAGTCAAGGGCATCAGTGTGGTCA[C/G]AGTGGCAACGGTTAGATTGGTGGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 604024 | ||||||||||||||||||||
Literature Links: |
SLC5A6 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 |
SLC5A6 - solute carrier family 5 member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_021095.2 | 1800 | Missense Mutation | CTG,GTG | L,V 504 | NP_066918.2 | |
XM_006712128.1 | 1800 | Missense Mutation | CTG,GTG | L,V 504 | XP_006712191.1 | |
XM_006712129.1 | 1800 | Missense Mutation | CTG,GTG | L,V 504 | XP_006712192.1 | |
XM_006712130.1 | 1800 | Missense Mutation | CTG,GTG | L,V 504 | XP_006712193.1 | |
XM_011533146.2 | 1800 | Missense Mutation | CTG,GTG | L,V 281 | XP_011531448.1 | |
XM_017005216.1 | 1800 | Missense Mutation | CTG,GTG | L,V 295 | XP_016860705.1 |