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NM_000057.4(BLM):c.3930T>G (p.Ser1310Arg) AND Hereditary cancer-predisposing syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Apr 5, 2024
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:
RCV002374537.4

Allele description [Variation Report for NM_000057.4(BLM):c.3930T>G (p.Ser1310Arg)]

NM_000057.4(BLM):c.3930T>G (p.Ser1310Arg)

Gene:
BLM:BLM RecQ like helicase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
15q26.1
Genomic location:
Preferred name:
NM_000057.4(BLM):c.3930T>G (p.Ser1310Arg)
HGVS:
  • NC_000015.10:g.90811260T>G
  • NG_007272.1:g.98889T>G
  • NM_000057.4:c.3930T>GMANE SELECT
  • NM_001287246.2:c.3930T>G
  • NM_001287247.2:c.3537T>G
  • NM_001287248.2:c.2805T>G
  • NP_000048.1:p.Ser1310Arg
  • NP_001274175.1:p.Ser1310Arg
  • NP_001274176.1:p.Ser1179Arg
  • NP_001274177.1:p.Ser935Arg
  • LRG_20t1:c.3930T>G
  • LRG_20:g.98889T>G
  • NC_000015.9:g.91354490T>G
  • NM_000057.2:c.3930T>G
  • NM_000057.3:c.3930T>G
Protein change:
S1179R
Links:
dbSNP: rs886051552
NCBI 1000 Genomes Browser:
rs886051552
Molecular consequence:
  • NM_000057.4:c.3930T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001287246.2:c.3930T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001287247.2:c.3537T>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001287248.2:c.2805T>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Hereditary cancer-predisposing syndrome
Synonyms:
Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002624304Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Apr 5, 2024) 		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, SCV002624304.4

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

Description

The c.3930T>G (p.S1310R) alteration is located in exon 21 (coding exon 20) of the BLM gene. This alteration results from a T to G substitution at nucleotide position 3930, causing the serine (S) at amino acid position 1310 to be replaced by an arginine (R). 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: Sep 29, 2024