KIAA1549L KIAA1549 like
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 20 |
not provided | 1 | 0 |
Uncertain significance | 0 | 182 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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210 |
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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
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 |
Search Word
Target data | : |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | C11orf41 |
SYNONYM | C11orf69 |
SYNONYM | G2 |
MIM | 612297 OMIM |
HGNC | HGNC:24836 HGNC |
Ensembl | ENSG00000110427 Ensembl |
AllianceGenome | HGNC:24836 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000526400.7 | hg38 | chr11 | 33,376,466 | 33,674,102 | 297,637 |
ENST00000658780.2 | hg38 | chr11 | 33,376,108 | 33,674,102 | 297,995 |
ENST00000321505.9 | hg38 | chr11 | 33,542,331 | 33,674,098 | 131,768 |
ENST00000658780.2 | hg19 | chr11 | 33,397,654 | 33,695,648 | 297,995 |
ENST00000526400.7 | hg19 | chr11 | 33,398,012 | 33,695,648 | 297,637 |
ENST00000321505.9 | hg19 | chr11 | 33,563,877 | 33,695,644 | 131,768 |
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