chrX:78011191:G>C Detail (hg38) (ATP7A, PGK1)

Go to:

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

Information

Genome

Assembly	Position
hg19	chrX:77,266,688-77,266,688 View the variant detail on this assembly version.
hg38	chrX:78,011,191-78,011,191

HGVS

ATP7A
PGK1

Type	Transcript	Protein
RefSeq	NM_000052.6:c.1885G>C	NP_000043.4:p.Ala629Pro
	NM_001282224.1:c.1915G>C	NP_001269153.1:p.Ala639Pro
Ensemble	ENST00000341514.11:c.1885G>C	ENST00000341514.11:p.Ala629Pro
	ENST00000343533.10:c.1915G>C	ENST00000343533.10:p.Ala639Pro
	ENST00000685264.1:c.1885G>C	ENST00000685264.1:p.Ala629Pro
	ENST00000686033.1:c.1885G>C	ENST00000686033.1:p.Ala629Pro
	ENST00000686133.1:c.1885G>C	ENST00000686133.1:p.Ala629Pro
	ENST00000686480.1:c.1885G>C	ENST00000686480.1:p.Ala629Pro
	ENST00000686543.1:c.1885G>C	ENST00000686543.1:p.Ala629Pro
	ENST00000686688.1:c.1885G>C	ENST00000686688.1:p.Ala629Pro
	ENST00000687086.1:c.1885G>C	ENST00000687086.1:p.Ala629Pro
	ENST00000689649.1:c.1885G>C	ENST00000689649.1:p.Ala629Pro
	ENST00000689767.1:c.1978G>C	ENST00000689767.1:p.Ala660Pro
	ENST00000692908.1:c.1885G>C	ENST00000692908.1:p.Ala629Pro
	ENST00000693398.1:c.1885G>C	ENST00000693398.1:p.Ala629Pro

Type	Transcript	Protein
RefSeq
Ensemble	ENST00000644362.1:c.-19-98676G>C

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Likely pathogenic
Review star
Show details

Links

ATP7A
PGK1

Type	Database	ID	Link
Gene	MIM	300011	OMIM
	HGNC	869	HGNC
	Ensembl	ENSG00000165240	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Type	Database	ID	Link
Gene	MIM	311800	OMIM
	HGNC	8896	HGNC
	Ensembl	ENSG00000102144	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
Likely pathogenic	2013-02-08	criteria provided, single submitter	Menkes kinky-hair syndrome	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.606	Menkes Kinky Hair Syndrome	NA	CLINVAR		Detail
0.606	Menkes Kinky Hair Syndrome	A numerical investigation into possible mechanisms by that the A629P mutant of A...	BeFree	20714486	Detail

Annotation

Annotations

Descrption	Source	Links
NM_000052.7(ATP7A):c.1885G>C (p.Ala629Pro) AND Menkes kinky-hair syndrome	ClinVar	Detail
NA	DisGeNET	Detail
A numerical investigation into possible mechanisms by that the A629P mutant of ATP7A causes Menkes D...	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: rs72554639 dbSNP
Genome: hg38
Position: chrX:78,011,191-78,011,191
Variant Type: snv
Reference Allele: G
Alternative Allele: C

Genome browser