NM_000204.5(CFI):c.1322A>G (p.Lys441Arg) AND Atypical hemolytic-uremic syndrome with I factor anomaly

Germline classification:: Benign (1 submission)
Last evaluated:: Jan 12, 2018
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:: RCV000325590.5

Allele description [Variation Report for NM_000204.5(CFI):c.1322A>G (p.Lys441Arg)]

NM_000204.5(CFI):c.1322A>G (p.Lys441Arg)

Gene:

CFI:complement factor I [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

4q25

Genomic location:

Preferred name:

NM_000204.5(CFI):c.1322A>G (p.Lys441Arg)

HGVS:

NC_000004.12:g.109746329T>C
NG_007569.1:g.60657A>G
NM_000204.5:c.1322A>GMANE SELECT
NM_001318057.2:c.1346A>G
NM_001331035.2:c.1301A>G
NM_001375278.1:c.1346A>G
NM_001375279.1:c.1322A>G
NM_001375280.1:c.1301A>G
NM_001375281.1:c.1322A>G
NM_001375282.1:c.1301A>G
NM_001375283.1:c.1265A>G
NM_001375284.1:c.713A>G
NP_000195.3:p.Lys441Arg
NP_001304986.2:p.Lys449Arg
NP_001317964.1:p.Lys434Arg
NP_001362207.1:p.Lys449Arg
NP_001362208.1:p.Lys441Arg
NP_001362209.1:p.Lys434Arg
NP_001362210.1:p.Lys441Arg
NP_001362211.1:p.Lys434Arg
NP_001362212.1:p.Lys422Arg
NP_001362213.1:p.Lys238Arg
LRG_48t1:c.1322A>G
LRG_48:g.60657A>G
NC_000004.11:g.110667485T>C
NM_000204.3:c.1322A>G
NM_000204.4:c.1322A>G
NR_164672.1:n.1372A>G
NR_164673.1:n.1346A>G

Protein change:

K238R

Links:

dbSNP: rs41278047

NCBI 1000 Genomes Browser:

rs41278047

Molecular consequence:

NM_000204.5:c.1322A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001318057.2:c.1346A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001331035.2:c.1301A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001375278.1:c.1346A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001375279.1:c.1322A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001375280.1:c.1301A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001375281.1:c.1322A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001375282.1:c.1301A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001375283.1:c.1265A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001375284.1:c.713A>G - missense variant - [Sequence Ontology: SO:0001583]
NR_164672.1:n.1372A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_164673.1:n.1346A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Atypical hemolytic-uremic syndrome with I factor anomaly
Synonyms:: HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3; AHUS, SUSCEPTIBILITY TO, 3; Atypical hemolytic-uremic syndrome 3
Identifiers:: MONDO: MONDO:0013041; MedGen: C2752039; Orphanet: 2134; OMIM: 612923

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000446871	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification Criteria 13 December 2019)	Benign (Jan 12, 2018)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000446871

Illumina Laboratory Services, Illumina

criteria provided, single submitter

(ICSL Variant Classification Criteria 13 December 2019)

Benign
(Jan 12, 2018)

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 Illumina Laboratory Services, Illumina, SCV000446871.3

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

Description

This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.

#	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: Oct 20, 2024

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