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ACACGAGGATGCATGCCAGCAGGGT[A/G]ACAGCCCACGGTGGGAGGCTGCTCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604309 | ||||||||||||||||||||
Literature Links: |
C7orf73 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 |
C7orf73 - chromosome 7 open reading frame 73 | ||||||
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There are no transcripts associated with this gene. |
SLC13A4 - solute carrier family 13 member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318192.1 | 2223 | Silent Mutation | GTC,GTT | V,V 505 | NP_001305121.1 | |
NM_012450.3 | 2223 | Silent Mutation | GTC,GTT | V,V 504 | NP_036582.2 | |
XM_011516024.2 | 2223 | Silent Mutation | GTC,GTT | V,V 505 | XP_011514326.1 | |
XM_017011962.1 | 2223 | Silent Mutation | GTC,GTT | V,V 453 | XP_016867451.1 | |
XM_017011963.1 | 2223 | Intron | XP_016867452.1 |