RBM38 RNA binding motif protein 38

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: RBM38
Type: protein-coding
Description: RNA binding motif protein 38
Entrez Gene ID: 55544
Genome: hg19
Position: chr20:55,966,452-55,984,389
Genome: hg38
Position: chr20:57,391,396-57,409,333
MIM: 612428 OMIM
HGNC: HGNC:15818 HGNC
Ensembl: ENSG00000132819 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	4
Likely benign	0	2
not provided	1	0
Uncertain significance	0	18

Ranking

	ClinVar
	0
	0
	0
	24
	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

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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
Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	Entry	Origin	Type	Annotation	Genome	Entry	Origin	Annotation	CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction

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
Name	Entry	Origin	Type	Annotation	Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Search Word

Target data	:	MGeND data only
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
Name	Entry	Origin	Type	Annotation	Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Type	ID
SYNONYM	HSRNASEB
SYNONYM	RNPC1
SYNONYM	SEB4B
SYNONYM	SEB4D
SYNONYM	dJ800J21.2
MIM	612428 OMIM
HGNC	HGNC:15818 HGNC
Ensembl	ENSG00000132819 Ensembl
AllianceGenome	HGNC:15818

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000356208.10	hg38	chr20	57,391,396	57,409,333	17,938
ENST00000371219.2	hg38	chr20	57,392,230	57,407,860	15,631
ENST00000440234.6	hg38	chr20	57,391,428	57,407,713	16,286
ENST00000344785.10	hg38	chr20	57,391,637	57,409,333	17,697
ENST00000356208.10	hg19	chr20	55,966,452	55,984,389	17,938
ENST00000440234.6	hg19	chr20	55,966,484	55,982,769	16,286
ENST00000344785.10	hg19	chr20	55,966,693	55,984,389	17,697
ENST00000371219.2	hg19	chr20	55,967,286	55,982,916	15,631

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