NM_001876.4(CPT1A):c.1164-119A>G AND not provided

Germline classification:: Benign (1 submission)
Last evaluated:: Mar 3, 2015
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:: RCV001718215.2

Allele description [Variation Report for NM_001876.4(CPT1A):c.1164-119A>G]

NM_001876.4(CPT1A):c.1164-119A>G

Genes:

LOC126861244:BRD4-independent group 4 enhancer GRCh37_chr11:68549035-68550234 [Gene]
CPT1A:carnitine palmitoyltransferase 1A [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q13.3

Genomic location:

Preferred name:

NM_001876.4(CPT1A):c.1164-119A>G

HGVS:

NC_000011.10:g.68782078T>C
NG_011801.1:g.64854A>G
NM_001031847.3:c.1164-119A>G
NM_001876.4:c.1164-119A>GMANE SELECT
NC_000011.9:g.68549546T>C

Links:

dbSNP: rs2305508

NCBI 1000 Genomes Browser:

rs2305508

Molecular consequence:

NM_001031847.3:c.1164-119A>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001876.4:c.1164-119A>G - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

Clear Turn Off Turn On

Work package 3.5: model-based analysis sensitivity analysis results - An interve...
Work package 3.5: model-based analysis sensitivity analysis results - An intervention to support adherence to inhaled medication in adults with cystic fibrosis: the ACtiF research programme including RCT
GALNT8 [Egretta garzetta]
GALNT8 [Egretta garzetta]
Gene ID:104124184

Gene

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001943601	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Benign (Mar 3, 2015)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001943601

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Benign
(Mar 3, 2015)

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	yes	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From GeneDx, SCV001943601.2

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

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

Last Updated: Dec 24, 2023

ClinVar

Relating variation to medicine