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GGTACCTGGACCTCCTGACCACGTG[A/G]TACTGCAGCTTCAAAGACTGCTGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
10 submissions
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Phenotype: |
MIM: 611063 MIM: 607555 | ||||||||||||||||||||
Literature Links: |
FAM20B 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 |
FAM20B - family with sequence similarity 20 member B | ||||||
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There are no transcripts associated with this gene. |
TOR3A - torsin family 3 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022371.3 | 464 | Missense Mutation | TGA,TGG | *,W 104 | NP_071766.2 |