U.S. flag

An official website of the United States government

NM_022168.4(IFIH1):c.2105C>T (p.Thr702Ile) AND Aicardi-Goutieres syndrome 7

Germline classification:
Likely benign (1 submission)
Last evaluated:
Jun 30, 2020
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:
RCV002272314.3

Allele description [Variation Report for NM_022168.4(IFIH1):c.2105C>T (p.Thr702Ile)]

NM_022168.4(IFIH1):c.2105C>T (p.Thr702Ile)

Gene:
IFIH1:interferon induced with helicase C domain 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2q24.2
Genomic location:
Preferred name:
NM_022168.4(IFIH1):c.2105C>T (p.Thr702Ile)
HGVS:
  • NC_000002.12:g.162276886G>A
  • NG_011495.1:g.46644C>T
  • NM_022168.4:c.2105C>TMANE SELECT
  • NP_071451.2:p.Thr702Ile
  • LRG_1235t1:c.2105C>T
  • LRG_1235:g.46644C>T
  • LRG_1235p1:p.Thr702Ile
  • NC_000002.11:g.163133396G>A
  • NM_022168.3:c.2105C>T
Protein change:
T702I
Links:
dbSNP: rs72650663
NCBI 1000 Genomes Browser:
rs72650663
Molecular consequence:
  • NM_022168.4:c.2105C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Aicardi-Goutieres syndrome 7 (AGS7)
Identifiers:
MONDO: MONDO:0014367; MedGen: C3888244; Orphanet: 51; OMIM: 615846

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV002556539Genetics and Molecular Pathology, SA Pathology

See additional submitters

criteria provided, single submitter

(ACMG Guidelines, 2015)
Likely benign
(Jun 30, 2020)
germlineclinical testing

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Genetics and Molecular Pathology, SA Pathology, SCV002556539.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 13, 2024