NM_017780.4(CHD7):c.6001G>A (p.Ala2001Thr) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Feb 28, 2024
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV004374087.1

Allele description [Variation Report for NM_017780.4(CHD7):c.6001G>A (p.Ala2001Thr)]

NM_017780.4(CHD7):c.6001G>A (p.Ala2001Thr)

Gene:

CHD7:chromodomain helicase DNA binding protein 7 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

8q12.2

Genomic location:

Preferred name:

NM_017780.4(CHD7):c.6001G>A (p.Ala2001Thr)

HGVS:

NC_000008.11:g.60852604G>A
NG_007009.1:g.178825G>A
NM_001316690.1:c.1717-9625G>A
NM_017780.3:c.6001G>A
NM_017780.4:c.6001G>AMANE SELECT
NP_060250.2:p.Ala2001Thr
NP_060250.2:p.Ala2001Thr
LRG_176t1:c.6001G>A
LRG_176:g.178825G>A
LRG_176p1:p.Ala2001Thr
NC_000008.10:g.61765163G>A
NM_017780.2:c.6001G>A

Protein change:

A2001T

Molecular consequence:

NM_001316690.1:c.1717-9625G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_017780.4:c.6001G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Inborn genetic diseases
Identifiers:: MeSH: D030342; MedGen: C0950123

Recent activity

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kelch repeat and BTB domain-containing protein 6 [Homo sapiens]
kelch repeat and BTB domain-containing protein 6 [Homo sapiens]
gi|45333883|ref|NP_690867.3|

Protein

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004923871	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Feb 28, 2024)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004923871

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Feb 28, 2024)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV004923871.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

The c.6001G>A (p.A2001T) alteration is located in exon 30 (coding exon 29) of the CHD7 gene. This alteration results from a G to A substitution at nucleotide position 6001, causing the alanine (A) at amino acid position 2001 to be replaced by a threonine (T). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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