SNHG32 small nucleolar RNA host gene 32
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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
Search Word
Target data | : |
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 | C6orf48 |
SYNONYM | D6S57 |
SYNONYM | G8 |
MIM | 605447 OMIM |
HGNC | HGNC:19078 HGNC |
Ensembl | ENSG00000204387 Ensembl |
AllianceGenome | HGNC:19078 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000375638.7 | hg38 | chr6 | 31,834,908 | 31,839,761 | 4,854 |
ENST00000614363.4 | hg38 | chr6 | 31,834,922 | 31,839,766 | 4,845 |
ENST00000375642.6 | hg38 | chr6 | 31,834,918 | 31,839,761 | 4,844 |
ENST00000395788.3 | hg38 | chr6 | 31,836,843 | 31,839,764 | 2,922 |
ENST00000395789.5 | hg38 | chr6 | 31,834,932 | 31,839,761 | 4,830 |
ENST00000375638.7 | hg19 | chr6 | 31,802,685 | 31,807,538 | 4,854 |
ENST00000375642.6 | hg19 | chr6 | 31,802,695 | 31,807,538 | 4,844 |
ENST00000614363.4 | hg19 | chr6 | 31,802,699 | 31,807,543 | 4,845 |
ENST00000395789.5 | hg19 | chr6 | 31,802,709 | 31,807,538 | 4,830 |
ENST00000395788.3 | hg19 | chr6 | 31,804,620 | 31,807,541 | 2,922 |
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