NM_000492.4(CFTR):c.3403T>C (p.Leu1135=) AND Cystic fibrosis

Germline classification:: Likely benign (1 submission)
Last evaluated:: Sep 9, 2022
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:: RCV002686064.3

Allele description [Variation Report for NM_000492.4(CFTR):c.3403T>C (p.Leu1135=)]

NM_000492.4(CFTR):c.3403T>C (p.Leu1135=)

Gene:

CFTR:CF transmembrane conductance regulator [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7q31.2

Genomic location:

Preferred name:

NM_000492.4(CFTR):c.3403T>C (p.Leu1135=)

HGVS:

NC_000007.14:g.117614648T>C
NG_016465.4:g.153865T>C
NM_000492.4:c.3403T>CMANE SELECT
NP_000483.3:p.Leu1135=
NP_000483.3:p.Leu1135=
LRG_663t1:c.3403T>C
LRG_663:g.153865T>C
LRG_663p1:p.Leu1135=
NC_000007.13:g.117254702T>C
NM_000492.3:c.3403T>C

Molecular consequence:

NM_000492.4:c.3403T>C - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: Cystic fibrosis (CF)
Synonyms:: Mucoviscidosis
Identifiers:: MONDO: MONDO:0009061; MedGen: C0010674; Orphanet: 586; OMIM: 219700

Recent activity

Clear Turn Off Turn On

Klebsiella variicola strain Kp_HUCA_Bac_59 NODE_166_length_456242_cov_60.034355,...
Klebsiella variicola strain Kp_HUCA_Bac_59 NODE_166_length_456242_cov_60.034355, whole genome shotgun sequence
gi|2154551521|ref|NZ_JAGKYQ01000006 gnl|WGS:NZ_JAGKYQ01|NODE_166_length_456242_cov_60.034355

Nucleotide
polyadenylate-binding protein-interacting protein 2 [Cephus cinctus]
polyadenylate-binding protein-interacting protein 2 [Cephus cinctus]
gi|1000744236|ref|XP_015594825.1|

Protein
MULTISPECIES: type II toxin-antitoxin system RelB/DinJ family antitoxin [Lactoba...
MULTISPECIES: type II toxin-antitoxin system RelB/DinJ family antitoxin [Lactobacillales]
gi|489756227|ref|WP_003660204.1|

Protein
MULTISPECIES: recombinase family protein [Lactobacillaceae]
MULTISPECIES: recombinase family protein [Lactobacillaceae]
gi|1821964574|ref|WP_165709795.1|

Protein
calcium/calmodulin-dependent protein kinase type II subunit beta isoform X24 [Ho...
calcium/calmodulin-dependent protein kinase type II subunit beta isoform X24 [Homo sapiens]
gi|1034657022|ref|XP_016868154.1|

Protein

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
SCV002996769	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Sep 9, 2022)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002996769

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Sep 9, 2022)

germline

clinical testing

PubMed (1)
[See all records that cite this PMID]

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV002996769.2

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

#	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

ClinVar

Relating variation to medicine