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GTCCTGAGTGACCCCAGGAGTGGCA[T/C]GTAGGTGACACGGTGTCGAGTCAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610300 MIM: 187270 | ||||||||||||||||||||
Literature Links: |
SLC6A18 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 |
SLC6A18 - solute carrier family 6 member 18 | ||||||
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There are no transcripts associated with this gene. |
TERT - telomerase reverse transcriptase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193376.1 | 3137 | Missense Mutation | ATG,GTG | M,V 1027 | NP_001180305.1 | |
NM_198253.2 | 3137 | Missense Mutation | ATG,GTG | M,V 1090 | NP_937983.2 | |
XM_017009796.1 | 3137 | Missense Mutation | ATG,GTG | M,V 1300 | XP_016865285.1 |