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NM_005535.3(IL12RB1):c.1912C>T (p.Pro638Ser) AND Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jul 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:
RCV001217741.7

Allele description [Variation Report for NM_005535.3(IL12RB1):c.1912C>T (p.Pro638Ser)]

NM_005535.3(IL12RB1):c.1912C>T (p.Pro638Ser)

Gene:
IL12RB1:interleukin 12 receptor subunit beta 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
19p13.11
Genomic location:
Preferred name:
NM_005535.3(IL12RB1):c.1912C>T (p.Pro638Ser)
HGVS:
  • NC_000019.10:g.18059965G>A
  • NG_007366.2:g.43985C>T
  • NM_001290023.2:c.1912C>T
  • NM_001290024.1:c.2032C>T
  • NM_005535.1:c.1912C>T
  • NM_005535.3:c.1912C>TMANE SELECT
  • NP_001276952.1:p.Pro638Ser
  • NP_001276953.1:p.Pro678Ser
  • NP_005526.1:p.Pro638Ser
  • LRG_72t1:c.1912C>T
  • LRG_72:g.43985C>T
  • NC_000019.9:g.18170775G>A
  • NM_005535.2:c.1912C>T
Protein change:
P638S
Links:
dbSNP: rs1327805116
NCBI 1000 Genomes Browser:
rs1327805116
Molecular consequence:
  • NM_001290023.2:c.1912C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001290024.1:c.2032C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_005535.3:c.1912C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency
Synonyms:
IL12RB1 DEFICIENCY; Immunodeficiency 30
Identifiers:
MONDO: MONDO:0013955; MedGen: C4013949; Orphanet: 319552; OMIM: 614891

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001389593Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Jul 24, 2022) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical 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, SCV001389593.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

This sequence change replaces proline, which is neutral and non-polar, with serine, which is neutral and polar, at codon 638 of the IL12RB1 protein (p.Pro638Ser). The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This variant has not been reported in the literature in individuals affected with IL12RB1-related conditions. ClinVar contains an entry for this variant (Variation ID: 946802). Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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

Last Updated: Sep 29, 2024