NM_000404.4(GLB1):c.396+122C>A AND not provided

Germline classification:: Benign (2 submissions)
Last evaluated:: Jun 19, 2018
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:: RCV000837640.2

Allele description [Variation Report for NM_000404.4(GLB1):c.396+122C>A]

NM_000404.4(GLB1):c.396+122C>A

Gene:

GLB1:galactosidase beta 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3p22.3

Genomic location:

Preferred name:

NM_000404.4(GLB1):c.396+122C>A

HGVS:

NC_000003.12:g.33068698G>T
NG_009005.1:g.33505C>A
NM_000404.4:c.396+122C>AMANE SELECT
NM_001079811.3:c.306+122C>A
NM_001135602.3:c.246-3141C>A
NM_001317040.2:c.540+122C>A
NM_001393580.1:c.396+122C>A
NC_000003.11:g.33110190G>T
NM_000404.2:c.396+122C>A

Links:

dbSNP: rs11129543

NCBI 1000 Genomes Browser:

rs11129543

Molecular consequence:

NM_000404.4:c.396+122C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001079811.3:c.306+122C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001135602.3:c.246-3141C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001317040.2:c.540+122C>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001393580.1:c.396+122C>A - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

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plasma membrane calcium-transporting ATPase 4 isoform X1 [Gallus gallus]
plasma membrane calcium-transporting ATPase 4 isoform X1 [Gallus gallus]
gi|2024386320|ref|XP_040508978.1|

Protein
PREDICTED: Homo sapiens galactosidase beta 1 like (GLB1L), transcript variant X6...
PREDICTED: Homo sapiens galactosidase beta 1 like (GLB1L), transcript variant X6, mRNA
gi|2462577070|ref|XM_054343871.1|

Nucleotide
Homo sapiens replication protein A1 (RPA1), transcript variant 2, mRNA
Homo sapiens replication protein A1 (RPA1), transcript variant 2, mRNA
gi|1676441050|ref|NM_001355120.2|

Nucleotide
CBTC3210.rev NICHD_XGC_tropBone1 Xenopus tropicalis cDNA clone IMAGE:8935453 3',...
CBTC3210.rev NICHD_XGC_tropBone1 Xenopus tropicalis cDNA clone IMAGE:8935453 3', mRNA sequence
gi|126264113|gnl|dbEST|45037777|gb| 225.1|

Nucleotide
Dothideomycetes RNA polymerase II second largest subunit (RPB2) gene, partial cd...
Dothideomycetes RNA polymerase II second largest subunit (RPB2) gene, partial cds.
PopSet: 291419541

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000979500	GeneDx	criteria provided, single submitter (GeneDx Variant Classification (06012015))	Benign (Jun 19, 2018)	germline	clinical testing	Citation Link,
SCV005245084	Breakthrough Genomics, Breakthrough Genomics	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign	germline	not provided	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000979500

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification (06012015))

Benign
(Jun 19, 2018)

germline

clinical testing

Citation Link,

SCV005245084

Breakthrough Genomics, Breakthrough Genomics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign

germline

not provided

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

Citations

PubMed

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 GeneDx, SCV000979500.1

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

Description

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

#	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 Breakthrough Genomics, Breakthrough Genomics, SCV005245084.1

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

#	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

Last Updated: Sep 29, 2024

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