U.S. flag

An official website of the United States government

NM_000135.4(FANCA):c.4188A>G (p.Ile1396Met) AND Inborn genetic diseases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Nov 17, 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:
RCV004036022.1

Allele description [Variation Report for NM_000135.4(FANCA):c.4188A>G (p.Ile1396Met)]

NM_000135.4(FANCA):c.4188A>G (p.Ile1396Met)

Genes:
FANCA:FA complementation group A [Gene - OMIM - HGNC]
ZNF276:zinc finger protein 276 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
16q24.3
Genomic location:
Preferred name:
NM_000135.4(FANCA):c.4188A>G (p.Ile1396Met)
Other names:
p.Ile1396Met
HGVS:
  • NC_000016.10:g.89738954T>C
  • NG_011706.1:g.82704A>G
  • NM_000135.4:c.4188A>GMANE SELECT
  • NM_001113525.2:c.*708T>CMANE SELECT
  • NM_001286167.3:c.4192A>G
  • NM_152287.4:c.*708T>C
  • NP_000126.2:p.Ile1396Met
  • NP_000126.2:p.Ile1396Met
  • NP_001273096.1:p.Asn1398Asp
  • LRG_495t1:c.4188A>G
  • LRG_495:g.82704A>G
  • LRG_495p1:p.Ile1396Met
  • NC_000016.9:g.89805362T>C
  • NM_000135.2:c.4188A>G
  • NM_000135.2:c.4188A>G
  • NR_110122.2:n.2708T>C
  • NR_110126.2:n.2591T>C
  • NR_110128.2:n.2531T>C
  • NR_110129.2:n.2625T>C
Protein change:
I1396M
Links:
dbSNP: rs1441175300
NCBI 1000 Genomes Browser:
rs1441175300
Molecular consequence:
  • NM_001113525.2:c.*708T>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_152287.4:c.*708T>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_000135.4:c.4188A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001286167.3:c.4192A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NR_110122.2:n.2708T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_110126.2:n.2591T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_110128.2:n.2531T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_110129.2:n.2625T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Inborn genetic diseases
Identifiers:
MeSH: D030342; MedGen: C0950123

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004869473Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Nov 17, 2023) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV004869473.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The c.4188A>G (p.I1396M) alteration is located in exon 42 (coding exon 42) of the FANCA gene. This alteration results from a A to G substitution at nucleotide position 4188, causing the isoleucine (I) at amino acid position 1396 to be replaced by a methionine (M). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 20, 2024