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TCTCCTGGCTTCTTACTCAGTCCAT[C/T]TTCTGCTTAGTATGTGTATTCAGAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616518 MIM: 611023 | ||||||||||||||||||||
Literature Links: |
SLC38A6 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 |
SLC38A6 - solute carrier family 38 member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001172702.1 | 399 | Missense Mutation | CTT,TTT | L,F 95 | NP_001166173.1 | |
NM_153811.2 | 399 | Missense Mutation | CTT,TTT | L,F 95 | NP_722518.2 | |
XM_006720049.3 | 399 | Missense Mutation | CTT,TTT | L,F 95 | XP_006720112.1 | |
XM_006720050.1 | 399 | Intron | XP_006720113.1 | |||
XM_011536469.2 | 399 | Missense Mutation | CTT,TTT | L,F 95 | XP_011534771.1 | |
XM_017021020.1 | 399 | Missense Mutation | CTT,TTT | L,F 95 | XP_016876509.1 | |
XM_017021021.1 | 399 | Missense Mutation | CTT,TTT | L,F 95 | XP_016876510.1 | |
XM_017021022.1 | 399 | Missense Mutation | CTT,TTT | L,F 72 | XP_016876511.1 | |
XM_017021023.1 | 399 | Missense Mutation | CTT,TTT | L,F 95 | XP_016876512.1 | |
XM_017021024.1 | 399 | Missense Mutation | CTT,TTT | L,F 95 | XP_016876513.1 | |
XM_017021025.1 | 399 | Missense Mutation | CTT,TTT | L,F 41 | XP_016876514.1 | |
XM_017021026.1 | 399 | Missense Mutation | CTT,TTT | L,F 41 | XP_016876515.1 | |
XM_017021027.1 | 399 | Intron | XP_016876516.1 | |||
XM_017021028.1 | 399 | Intron | XP_016876517.1 |
TRMT5 - tRNA methyltransferase 5 | ||||||
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There are no transcripts associated with this gene. |