chr2:38071044:G>T Detail (hg38) (CYP1B1)

Go to:

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

Information

Genome

Assembly	Position
hg19	chr2:38,298,187-38,298,187 View the variant detail on this assembly version.
hg38	chr2:38,071,044-38,071,044

HGVS

CYP1B1

Type	Transcript	Protein
RefSeq	NM_000104.3:c.1310C>A	NP_000095.2:p.Pro437Gln
Ensemble	ENST00000490576.2:c.1310C>A	ENST00000490576.2:p.Pro437Gln
	ENST00000494864.1:c.197C>A	ENST00000494864.1:p.Pro66Gln
	ENST00000610745.5:c.1310C>A	ENST00000610745.5:p.Pro437Gln
	ENST00000614273.1:c.1310C>A	ENST00000614273.1:p.Pro437Gln
	ENST00000714520.1:c.1310C>A	ENST00000714520.1:p.Pro437Gln

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

JP	HGVD:[No Data.]
	ToMMo:[No Data.]
	NCBN:[No Data.]
	NCBN(Hondo):[No Data.]
	NCBN(Ryukyu):[No Data.]
East asia	ExAC:<0.001

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	Five missense mutations associated with congenital glaucoma (Gly61Glu, Gly365Trp...	BeFree	12807732	Detail
0.320	GLAUCOMA 3, PRIMARY CONGENITAL, A	Molecular genetics of primary congenital glaucoma in Brazil.	UNIPROT	12036985	Detail
0.366	Glaucoma, Primary Open Angle	One each of POAG and PCG patients was detected to be heterozygous for CYP1B1 mut...	BeFree	15723004	Detail
0.025	primary congenital glaucoma	One each of POAG and PCG patients was detected to be heterozygous for CYP1B1 mut...	BeFree	15723004	Detail

Annotation

Annotations

Descrption	Source	Links
Five missense mutations associated with congenital glaucoma (Gly61Glu, Gly365Trp, Asp374Asn, Pro437L...	DisGeNET	Detail
Molecular genetics of primary congenital glaucoma in Brazil.	DisGeNET	Detail
One each of POAG and PCG patients was detected to be heterozygous for CYP1B1 mutation (c.1656C>T,...	DisGeNET	Detail
One each of POAG and PCG patients was detected to be heterozygous for CYP1B1 mutation (c.1656C>T,...	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: -
Genome: hg38
Position: chr2:38,071,044-38,071,044
Variant Type: snv
Reference Allele: G
Alternative Allele: T
East Asian Chromosome Counts (ExAC): 8654
East Asian Allele Counts (ExAC): 0
East Asian Heterozygous Counts (ExAC): 0
East Asian Homozygous Counts (ExAC): 0
East Asian Allele Frequency (ExAC): 0.0
Chromosome Counts in All Race (ExAC): 121396
Allele Counts in All Race (ExAC): 2
Heterozygous Counts in All Race (ExAC): 2
Homozygous Counts in All Race (ExAC): 0
Allele Frequency in All Race (ExAC): 1.6475007413753334E-5

Genome browser