HNRNPD heterogeneous nuclear ribonucleoprotein D

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
Locus Zoom
Variants
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Information

Symbol: HNRNPD
Type: protein-coding
Description: heterogeneous nuclear ribonucleoprotein D
Entrez Gene ID: 3184
Genome: hg19
Position: chr4:83,273,651-83,295,144
Genome: hg38
Position: chr4:82,352,498-82,373,991
MIM: 601324 OMIM
HGNC: HGNC:5036 HGNC
Ensembl: ENSG00000138668 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	0	2
Benign	0	16
Likely benign	0	4
Conflicting classifications of pathogenicity	0	2
Uncertain significance	0	24

Ranking

	ClinVar
	0
	0
	0
	46
	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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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

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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

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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
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	AUF1
SYNONYM	AUF1A
SYNONYM	HNRPD
SYNONYM	P37
SYNONYM	hnRNPD0
MIM	601324 OMIM
HGNC	HGNC:5036 HGNC
Ensembl	ENSG00000138668 Ensembl
AllianceGenome	HGNC:5036

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000703969.1	hg38	chr4	82,353,829	82,374,175	20,347
ENST00000703968.1	hg38	chr4	82,353,829	82,373,999	20,171
ENST00000353341.8	hg38	chr4	82,353,829	82,373,986	20,158
ENST00000703970.1	hg38	chr4	82,353,829	82,374,185	20,357
ENST00000313899.12	hg38	chr4	82,352,498	82,373,991	21,494
ENST00000503822.2	hg38	chr4	82,354,204	82,374,161	19,958
ENST00000352301.8	hg38	chr4	82,353,834	82,373,983	20,150
ENST00000313899.12	hg19	chr4	83,273,651	83,295,144	21,494
ENST00000353341.8	hg19	chr4	83,274,982	83,295,139	20,158
ENST00000352301.8	hg19	chr4	83,274,987	83,295,136	20,150
ENST00000503822.2	hg19	chr4	83,275,357	83,295,314	19,958
ENST00000703968.1	hg19	chr4	83,274,982	83,295,152	20,171
ENST00000703969.1	hg19	chr4	83,274,982	83,295,328	20,347
ENST00000703970.1	hg19	chr4	83,274,982	83,295,338	20,357

Key	Value
strand	-
start	83,274,466
Gene Symbol	HNRNPD
Entrez GeneId	3,184
Chr Band	4q21
end	83,295,148
chr	chr4

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