NM_001854.4(COL11A1):c.5231A>G (p.Tyr1744Cys) AND not provided

Germline classification:: Benign (1 submission)
Last evaluated:: Feb 24, 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:: RCV002040508.6

Allele description [Variation Report for NM_001854.4(COL11A1):c.5231A>G (p.Tyr1744Cys)]

NM_001854.4(COL11A1):c.5231A>G (p.Tyr1744Cys)

Genes:

LOC126805814:P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:103344928-103346127 [Gene]
COL11A1:collagen type XI alpha 1 chain [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p21.1

Genomic location:

Preferred name:

NM_001854.4(COL11A1):c.5231A>G (p.Tyr1744Cys)

HGVS:

NC_000001.11:g.102879726T>C
NG_008033.2:g.233771A>G
NM_001190709.2:c.5114A>G
NM_001854.4:c.5231A>GMANE SELECT
NM_080629.3:c.5267A>G
NM_080630.4:c.4883A>G
NP_001177638.1:p.Tyr1705Cys
NP_001845.3:p.Tyr1744Cys
NP_542196.2:p.Tyr1756Cys
NP_542197.3:p.Tyr1628Cys
NC_000001.10:g.103345282T>C
NR_134980.2:n.5591A>G

Protein change:

Y1628C

Links:

dbSNP: rs769329430

NCBI 1000 Genomes Browser:

rs769329430

Molecular consequence:

NM_001190709.2:c.5114A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001854.4:c.5231A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_080629.3:c.5267A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_080630.4:c.4883A>G - missense variant - [Sequence Ontology: SO:0001583]
NR_134980.2:n.5591A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

Clear Turn Off Turn On

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
SCV002297935	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Benign (Feb 24, 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

SCV002297935

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Benign
(Feb 24, 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, SCV002297935.3

#	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