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TGACCCTCGCCCATGCTGGGTAAGT[G/T]TCCAGGTGGAAGAGGCTAACTCCCC
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 | |||
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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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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 | 2544 | Missense Mutation | GAA,GAC | E,D 612 | NP_001305121.1 | |
NM_012450.3 | 2544 | Missense Mutation | GAA,GAC | E,D 611 | NP_036582.2 | |
XM_011516024.2 | 2544 | Missense Mutation | GAA,GAC | E,D 566 | XP_011514326.1 | |
XM_017011962.1 | 2544 | Missense Mutation | GAA,GAC | E,D 560 | XP_016867451.1 | |
XM_017011963.1 | 2544 | Intron | XP_016867452.1 |