chr7:117530983:G>T Detail (hg38) (CFTR)

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

Genome

Assembly	Position
hg19	chr7:117,171,037-117,171,037 View the variant detail on this assembly version.
hg38	chr7:117,530,983-117,530,983

HGVS

CFTR

Type	Transcript	Protein
RefSeq	NM_000492.3:c.358G>T	NP_000483.3:p.Ala120Ser
Ensemble	ENST00000003084.11:c.358G>T	ENST00000003084.11:p.Ala120Ser
	ENST00000648260.1:c.358G>T	ENST00000648260.1:p.Ala120Ser
	ENST00000649406.1:c.358G>T	ENST00000649406.1:p.Ala120Ser
	ENST00000649781.2:c.358G>T	ENST00000649781.2:p.Ala120Ser
	ENST00000699596.1:c.358G>T	ENST00000699596.1:p.Ala120Ser
	ENST00000699597.1:c.358G>T	ENST00000699597.1:p.Ala120Ser
	ENST00000699602.1:c.358G>T	ENST00000699602.1:p.Ala120Ser
	ENST00000699605.1:c.115G>T	ENST00000699605.1:p.Ala39Ser

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

CFTR

Type	Database	ID	Link
Gene	MIM	602421	OMIM
	HGNC	1884	HGNC
	Ensembl	ENSG00000001626	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
0.800	cystic fibrosis	The cystic fibrosis transmembrane regulator (CFTR) gene mutations identified wer...	BeFree	11883825	Detail

Annotation

Annotations

Descrption	Source	Links
The cystic fibrosis transmembrane regulator (CFTR) gene mutations identified were delF508, D1152H, R...	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: chr7:117,530,983-117,530,983
Variant Type: snv
Reference Allele: G
Alternative Allele: T
East Asian Chromosome Counts (ExAC): 8612
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): 120358
Allele Counts in All Race (ExAC): 1
Heterozygous Counts in All Race (ExAC): 1
Homozygous Counts in All Race (ExAC): 0
Allele Frequency in All Race (ExAC): 8.30854617059107E-6

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