NM_003721.4(RFXANK):c.188-11C>T AND MHC class II deficiency

This record was updated by the submitter. Please see the current version.

Germline classification:: Benign/Likely benign (4 submissions)
Last evaluated:: Jan 25, 2024
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV000985221.12

Allele description

NM_003721.4(RFXANK):c.188-11C>T

Gene:

RFXANK:regulatory factor X associated ankyrin containing protein [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.11

Genomic location:

Preferred name:

NM_003721.4(RFXANK):c.188-11C>T

HGVS:

NC_000019.10:g.19196952C>T
NG_007432.1:g.9754C>T
NM_001278727.2:c.188-11C>T
NM_001278728.2:c.188-14C>T
NM_001370233.1:c.188-11C>T
NM_001370234.1:c.188-11C>T
NM_001370235.1:c.188-14C>T
NM_001370236.1:c.188-14C>T
NM_001370237.1:c.188-14C>T
NM_001370238.1:c.188-11C>T
NM_003721.4:c.188-11C>TMANE SELECT
NM_134440.3:c.188-14C>T
LRG_102:g.9754C>T
NC_000019.9:g.19307761C>T
NM_003721.3:c.188-11C>T

Links:

dbSNP: rs201545133

NCBI 1000 Genomes Browser:

rs201545133

Molecular consequence:

NM_001278727.2:c.188-11C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001278728.2:c.188-14C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001370233.1:c.188-11C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001370234.1:c.188-11C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001370235.1:c.188-14C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001370236.1:c.188-14C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001370237.1:c.188-14C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001370238.1:c.188-11C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_003721.4:c.188-11C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_134440.3:c.188-14C>T - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:: MHC class II deficiency
Synonyms:: BLS, TYPE II; SCID, HLA CLASS II-NEGATIVE; Bare Lymphocyte Syndrome; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0008855; MedGen: C2931418; Orphanet: 572; OMIM: PS209920

Recent activity

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NIF3-like protein 1 isoform 2 [Rattus norvegicus]
NIF3-like protein 1 isoform 2 [Rattus norvegicus]
gi|67078492|ref|NP_001019934.1|

Protein
NIF3-like protein 1 isoform X3 [Rattus norvegicus]
NIF3-like protein 1 isoform X3 [Rattus norvegicus]
gi|2678970118|ref|XP_063123015.1|

Protein

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001133252	Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City	no assertion criteria provided	Uncertain significance (Sep 26, 2019)	germline	clinical testing
SCV001287269	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification Criteria 13 December 2019)	Likely benign (Jan 13, 2018)	germline	clinical testing	Citation Link,
SCV001729117	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Benign (Jan 25, 2024)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV002812617	Fulgent Genetics, Fulgent Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely benign (Mar 31, 2022)	unknown	clinical testing	PubMed (1) [See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	unknown	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing
not provided	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical 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

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 Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City, SCV001133252.1

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

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Illumina Laboratory Services, Illumina, SCV001287269.1

#	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 likely benign is not then subjected to further curation. The score for this variant resulted in a classification of likely 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

From Invitae, SCV001729117.4

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

#	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

From Fulgent Genetics, Fulgent Genetics, SCV002812617.1

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

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	unknown	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Jun 2, 2024

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