chr14:24258667:C>T Detail (hg38) (TGM1)

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

Genome

Assembly	Position
hg19	chr14:24,727,873-24,727,873 View the variant detail on this assembly version.
hg38	chr14:24,258,667-24,258,667

HGVS

TGM1

Type	Transcript	Protein
RefSeq	NM_000359.2:c.1166G>A	NP_000350.1:p.Arg389His
Ensemble	ENST00000206765.11:c.1166G>A	ENST00000206765.11:p.Arg389His
	ENST00000544573.5:c.-28-279G>A

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	Pathogenic Likely pathogenic
Review star
Show details

Links

TGM1

Type	Database	ID	Link
Gene	MIM	190195	OMIM
	HGNC	11777	HGNC
	Ensembl	ENSG00000092295	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar	tgv50173448	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2023-10-16	criteria provided, multiple submitters, no conflicts	autosomal recessive congenital ichthyosis 1	germline unknown	Detail
Pathogenic	2023-01-24	criteria provided, multiple submitters, no conflicts	not provided	germline	Detail
Likely pathogenic	2021-07-10	criteria provided, single submitter		germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.120	Ichthyosis Congenita II	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000359.3(TGM1):c.1166G>A (p.Arg389His) AND Autosomal recessive congenital ichthyosis 1	ClinVar	Detail
NM_000359.3(TGM1):c.1166G>A (p.Arg389His) AND not provided	ClinVar	Detail
NM_000359.3(TGM1):c.1166G>A (p.Arg389His) AND Abnormality of the skin	ClinVar	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: rs121918723 dbSNP
Genome: hg38
Position: chr14:24,258,667-24,258,667
Variant Type: snv
Reference Allele: C
Alternative Allele: T
East Asian Chromosome Counts (ExAC): 8648
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): 120942
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): 8.268426187759421E-6

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