NM_001374828.1(ARID1B):c.515A>C (p.His172Pro) AND not provided

Germline classification:: Likely benign (2 submissions)
Last evaluated:: Aug 17, 2023
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:: RCV001577105.4

Allele description [Variation Report for NM_001374828.1(ARID1B):c.515A>C (p.His172Pro)]

NM_001374828.1(ARID1B):c.515A>C (p.His172Pro)

Genes:

ARID1B:AT-rich interaction domain 1B [Gene - OMIM - HGNC]
LOC115308161:uncharacterized LOC115308161 [Gene]

Variant type:

single nucleotide variant

Cytogenetic location:

6q25.3

Genomic location:

Preferred name:

NM_001374828.1(ARID1B):c.515A>C (p.His172Pro)

HGVS:

NC_000006.12:g.156778195A>C
NG_066624.1:g.7170A>C
NM_001371656.1:c.515A>C
NM_001374820.1:c.515A>C
NM_001374828.1:c.515A>CMANE SELECT
NM_017519.3:c.515A>C
NM_020732.3:c.266A>C
NP_001358585.1:p.His172Pro
NP_001361749.1:p.His172Pro
NP_001361757.1:p.His172Pro
NP_059989.3:p.His172Pro
NC_000006.11:g.157099329A>C

Protein change:

H172P

Links:

dbSNP: rs757399076

NCBI 1000 Genomes Browser:

rs757399076

Molecular consequence:

NM_001371656.1:c.515A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001374820.1:c.515A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001374828.1:c.515A>C - missense variant - [Sequence Ontology: SO:0001583]
NM_017519.3:c.515A>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001804432	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Likely benign (Aug 6, 2020)	germline	clinical testing	Citation Link,
SCV004529870	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Aug 17, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001804432

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Likely benign
(Aug 6, 2020)

germline

clinical testing

Citation Link,

SCV004529870

Invitae

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Aug 17, 2023)

germline

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	germline	yes	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

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):240-242.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From GeneDx, SCV001804432.1

#	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 Invitae, SCV004529870.1

#	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	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Feb 28, 2024

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