chr12:101770477:T>G Detail (hg38) (GNPTAB)

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

Genome

Assembly	Position
hg19	chr12:102,164,255-102,164,255 View the variant detail on this assembly version.
hg38	chr12:101,770,477-101,770,477

HGVS

GNPTAB

Type	Transcript	Protein
RefSeq	NM_024312.4:c.1042A>C	NP_077288.2:p.Ile348Leu
Ensemble	ENST00000299314.12:c.1042A>C	ENST00000299314.12:p.Ile348Leu
	ENST00000549940.5:c.1042A>C	ENST00000549940.5:p.Ile348Leu

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	Benign Likely benign
Review star
Show details

Links

GNPTAB

Type	Database	ID	Link
Gene	MIM	607840	OMIM
	HGNC	29670	HGNC
	Ensembl	ENSG00000111670	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar	tgv380832116	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Likely benign	2019-05-28	criteria provided, multiple submitters, no conflicts	Mucolipidosis type II	germline unknown	Detail
Benign Likely benign	2021-12-10	criteria provided, multiple submitters, no conflicts	not specified	germline	Detail
Likely benign	2017-04-28	criteria provided, single submitter	Pseudo-Hurler polydystrophy	germline	Detail
Likely benign	2019-03-24	criteria provided, multiple submitters, no conflicts	not provided	germline unknown	Detail
Benign Likely benign	2024-02-01	criteria provided, multiple submitters, no conflicts	Mucolipidosis type II,Pseudo-Hurler polydystrophy	germline unknown	Detail
Benign Likely benign	2024-02-01	criteria provided, multiple submitters, no conflicts	Mucolipidosis type II,Pseudo-Hurler polydystrophy	germline unknown	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.441	MUCOLIPIDOSIS II ALPHA/BETA (disorder)	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_024312.5(GNPTAB):c.1042A>C (p.Ile348Leu) AND Mucolipidosis type II	ClinVar	Detail
NM_024312.5(GNPTAB):c.1042A>C (p.Ile348Leu) AND not specified	ClinVar	Detail
NM_024312.5(GNPTAB):c.1042A>C (p.Ile348Leu) AND Pseudo-Hurler polydystrophy	ClinVar	Detail
NM_024312.5(GNPTAB):c.1042A>C (p.Ile348Leu) AND not provided	ClinVar	Detail
NM_024312.5(GNPTAB):c.1042A>C (p.Ile348Leu) AND multiple conditions	ClinVar	Detail
NM_024312.5(GNPTAB):c.1042A>C (p.Ile348Leu) AND multiple conditions	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: rs7958709 dbSNP
Genome: hg38
Position: chr12:101,770,477-101,770,477
Variant Type: snv
Reference Allele: T
Alternative Allele: G
East Asian Chromosome Counts (ExAC): 8640
East Asian Allele Counts (ExAC): 1
East Asian Heterozygous Counts (ExAC): 1
East Asian Homozygous Counts (ExAC): 0
East Asian Allele Frequency (ExAC): 1.1574074074074075E-4
Chromosome Counts in All Race (ExAC): 121328
Allele Counts in All Race (ExAC): 455
Heterozygous Counts in All Race (ExAC): 447
Homozygous Counts in All Race (ExAC): 4
Allele Frequency in All Race (ExAC): 0.0037501648424106554

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