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TCTGCAGATGTCCTTCGGCCTTCTC[C/T]GTGTGTTCTCCATTGTGATCCCCTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614240 MIM: 602138 MIM: 615588 | ||||||||||||||||||||
Literature Links: |
FAM109B PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
FAM109B - family with sequence similarity 109 member B | ||||||
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There are no transcripts associated with this gene. |
NDUFA6 - NADH:ubiquinone oxidoreductase subunit A6 | ||||||
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There are no transcripts associated with this gene. |
NDUFA6-AS1 - NDUFA6 antisense RNA 1 (head to head) | ||||||
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There are no transcripts associated with this gene. |
SMDT1 - single-pass membrane protein with aspartate rich tail 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_033318.4 | 287 | Missense Mutation | CGT,TGT | R,C 69 | NP_201575.3 | |
XM_011530509.2 | 287 | Missense Mutation | CGT,TGT | R,C 69 | XP_011528811.1 |
SNORD13P1 - small nucleolar RNA, C/D box 13 pseudogene 1 | ||||||
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There are no transcripts associated with this gene. |