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TAACACAGCCTGGGGCTGTGCAGCT[A/G]CTCCTTCCGCCCCACCGGGCAGGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616525 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C17orf89 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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C17orf89 - chromosome 17 open reading frame 89 | ||||||
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There are no transcripts associated with this gene. |
SLC38A10 - solute carrier family 38 member 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001037984.2 | 2655 | Missense Mutation | GCA,GTA | A,V 948 | NP_001033073.1 | |
NM_138570.3 | 2655 | Intron | NP_612637.1 | |||
XM_005257019.1 | 2655 | Missense Mutation | GCA,GTA | A,V 956 | XP_005257076.1 | |
XM_011524288.1 | 2655 | Missense Mutation | GCA,GTA | A,V 963 | XP_011522590.1 | |
XM_011524289.1 | 2655 | Missense Mutation | GCA,GTA | A,V 955 | XP_011522591.1 | |
XM_011524290.1 | 2655 | Missense Mutation | GCA,GTA | A,V 874 | XP_011522592.1 |
TEPSIN - TEPSIN, adaptor related protein complex 4 accessory protein | ||||||
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There are no transcripts associated with this gene. |