TMT1A thiol methyltransferase 1A
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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22 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
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MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | AAM-B |
SYNONYM | AAMB |
SYNONYM | METTL7A |
MIM | 618338 OMIM |
HGNC | HGNC:24550 HGNC |
Ensembl | ENSG00000185432 Ensembl |
AllianceGenome | HGNC:24550 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000332160.5 | hg38 | chr12 | 50,925,015 | 50,932,508 | 7,494 |
ENST00000548553.1 | hg38 | chr12 | 50,923,472 | 50,932,510 | 9,039 |
ENST00000548553.1 | hg19 | chr12 | 51,317,255 | 51,326,293 | 9,039 |
ENST00000332160.5 | hg19 | chr12 | 51,318,798 | 51,326,291 | 7,494 |
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