chr2:38302361:C>G Detail (hg19) (CYP1B1)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr2:38,302,361-38,302,361
hg38	chr2:38,075,218-38,075,218 View the variant detail on this assembly version.

HGVS

CYP1B1

Type	Transcript	Protein
RefSeq	NM_000104.3:c.171G>C	NP_000095.2:p.Trp57Cys
Ensemble	ENST00000490576.2:c.171G>C	ENST00000490576.2:p.Trp57Cys
	ENST00000494864.1:c.-70-3908G>C
	ENST00000610745.5:c.171G>C	ENST00000610745.5:p.Trp57Cys
	ENST00000614273.1:c.171G>C	ENST00000614273.1:p.Trp57Cys
	ENST00000714520.1:c.171G>C	ENST00000714520.1:p.Trp57Cys

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star	[No Data.]
Show details

Links

CYP1B1

Type	Database	ID	Link
Gene	MIM	601771	OMIM
	HGNC	2597	HGNC
	Ensembl	ENSG00000138061	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

[No Data.]

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.135	hydrophthalmos	NA	CLINVAR		Detail
0.361	Irido-corneo-trabecular dysgenesis (disorder)	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NA	DisGeNET	Detail
NA	DisGeNET	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs72549387 dbSNP
Genome: hg19
Position: chr2:38,302,361-38,302,361
Variant Type: snv
Reference Allele: C
Alternative Allele: G

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