NM_001277115.2(DNAH11):c.2787C>G (p.Phe929Leu) AND Primary ciliary dyskinesia

Germline classification:: Benign (1 submission)
Last evaluated:: Aug 24, 2023
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:: RCV003538004.2

Allele description [Variation Report for NM_001277115.2(DNAH11):c.2787C>G (p.Phe929Leu)]

NM_001277115.2(DNAH11):c.2787C>G (p.Phe929Leu)

Gene:

DNAH11:dynein axonemal heavy chain 11 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7p15.3

Genomic location:

Preferred name:

NM_001277115.2(DNAH11):c.2787C>G (p.Phe929Leu)

HGVS:

NC_000007.14:g.21599906C>G
NG_012886.2:g.61692C>G
NM_001277115.2:c.2787C>GMANE SELECT
NM_003777.3:c.2787C>G
NP_001264044.1:p.Phe929Leu
NP_003768.2:p.Phe929Leu
NC_000007.13:g.21639524C>G

Protein change:

F929L

Molecular consequence:

NM_001277115.2:c.2787C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_003777.3:c.2787C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Primary ciliary dyskinesia
Synonyms:: Ciliary dyskinesia
Identifiers:: MONDO: MONDO:0016575; MedGen: C0008780; OMIM: PS244400; Human Phenotype Ontology: HP:0012265

Recent activity

Clear Turn Off Turn On

Homo sapiens collagen type XIII alpha 1 chain (COL13A1), transcript variant 1, m...
Homo sapiens collagen type XIII alpha 1 chain (COL13A1), transcript variant 1, mRNA
gi|1677498641|ref|NM_001130103.2|

Nucleotide
Homo sapiens collagen, type XIII, alpha 1 (COL13A1), transcript variant 9, mRNA
Homo sapiens collagen, type XIII, alpha 1 (COL13A1), transcript variant 9, mRNA
gi|18426940|ref|NM_080805.1|

Nucleotide
Salileptolyngbya diazotrophicum SCSIO 43686 16S ribosomal RNA gene, partial sequ...
Salileptolyngbya diazotrophicum SCSIO 43686 16S ribosomal RNA gene, partial sequence
gi|1407510710|gb|MF614799.1|

Nucleotide
Uncultured Salileptolyngbya sp. clone sle1 16S ribosomal RNA gene, partial seque...
Uncultured Salileptolyngbya sp. clone sle1 16S ribosomal RNA gene, partial sequence
gi|2717410587|gb|PP659392.1|

Nucleotide
Homo sapiens collagen type XIII alpha 1 chain (COL13A1), transcript variant 5, m...
Homo sapiens collagen type XIII alpha 1 chain (COL13A1), transcript variant 5, mRNA
gi|1677500089|ref|NM_080801.4|

Nucleotide

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
SCV004279814	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Benign (Aug 24, 2023)	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

SCV004279814

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Benign
(Aug 24, 2023)

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, SCV004279814.1

#	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