chr22:50625446:G>A Detail (hg38) (ARSA)

Go to:

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

Information

Genome

Assembly	Position
hg19	chr22:51,063,874-51,063,874 View the variant detail on this assembly version.
hg38	chr22:50,625,446-50,625,446

HGVS

ARSA

Type	Transcript	Protein
RefSeq	NM_000487.5:c.1229C>T	NP_000478.3:p.Thr410Ile
	NM_001085426.2:c.1229C>T	NP_001078895.2:p.Thr410Ile
	NM_001085427.2:c.1229C>T	NP_001078896.2:p.Thr410Ile
	NM_001085425.2:c.1229C>T	NP_001078894.2:p.Thr410Ile
	NM_001085428.2:c.971C>T	NP_001078897.1:p.Thr324Ile
Ensemble	ENST00000216124.10:c.1229C>T	ENST00000216124.10:p.Thr410Ile
	ENST00000356098.9:c.1229C>T	ENST00000356098.9:p.Thr410Ile
	ENST00000395619.3:c.1229C>T	ENST00000395619.3:p.Thr410Ile
	ENST00000395621.7:c.1229C>T	ENST00000395621.7:p.Thr410Ile
	ENST00000453344.6:c.971C>T	ENST00000453344.6:p.Thr324Ile

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	Likely pathogenic
Review star
Show details

Links

ARSA

Type	Database	ID	Link
Gene	MIM	607574	OMIM
	HGNC	713	HGNC
	Ensembl	ENSG00000100299	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

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2001-07-01	no assertion criteria provided	Metachromatic leukodystrophy, adult type	germline	Detail
Likely pathogenic	2023-11-06	criteria provided, single submitter	metachromatic leukodystrophy	germline not applicable	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.241	Metachromatic Leukodystrophy, Adult-Type (disorder)	NA	CLINVAR		Detail
0.514	Leukodystrophy, Metachromatic	We report the case of a 50-year-old woman and her 32-year-old daughter, both of ...	UNIPROT	11456299	Detail

Annotation

Annotations

Descrption	Source	Links
NM_000487.6(ARSA):c.1229C>T (p.Thr410Ile) AND Metachromatic leukodystrophy, adult type	ClinVar	Detail
NM_000487.6(ARSA):c.1229C>T (p.Thr410Ile) AND Metachromatic leukodystrophy	ClinVar	Detail
NA	DisGeNET	Detail
We report the case of a 50-year-old woman and her 32-year-old daughter, both of whom are affected wi...	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: rs28940895 dbSNP
Genome: hg38
Position: chr22:50,625,446-50,625,446
Variant Type: snv
Reference Allele: G
Alternative Allele: A
East Asian Chromosome Counts (ExAC): 8562
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): 112474
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): 8.890943684762701E-6

Genome browser