NM_000463.3(UGT1A1):c.584G>A (p.Arg195Lys) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 7, 2021
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:: RCV002556996.2

Allele description [Variation Report for NM_000463.3(UGT1A1):c.584G>A (p.Arg195Lys)]

NM_000463.3(UGT1A1):c.584G>A (p.Arg195Lys)

Genes:

UGT1A:UDP glucuronosyltransferase family 1 member A complex locus [Gene - HGNC]
UGT1A10:UDP glucuronosyltransferase family 1 member A10 [Gene - OMIM - HGNC]
UGT1A1:UDP glucuronosyltransferase family 1 member A1 [Gene - OMIM - HGNC]
UGT1A3:UDP glucuronosyltransferase family 1 member A3 [Gene - OMIM - HGNC]
UGT1A4:UDP glucuronosyltransferase family 1 member A4 [Gene - OMIM - HGNC]
UGT1A5:UDP glucuronosyltransferase family 1 member A5 [Gene - OMIM - HGNC]
UGT1A6:UDP glucuronosyltransferase family 1 member A6 [Gene - OMIM - HGNC]
UGT1A7:UDP glucuronosyltransferase family 1 member A7 [Gene - OMIM - HGNC]
UGT1A8:UDP glucuronosyltransferase family 1 member A8 [Gene - OMIM - HGNC]
UGT1A9:UDP glucuronosyltransferase family 1 member A9 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2q37.1

Genomic location:

Preferred name:

NM_000463.3(UGT1A1):c.584G>A (p.Arg195Lys)

HGVS:

NC_000002.12:g.233760871G>A
NG_002601.2:g.176128G>A
NG_033238.1:g.5599G>A
NM_000463.3:c.584G>AMANE SELECT
NM_001072.4:c.862-6163G>AMANE SELECT
NM_007120.3:c.868-6163G>AMANE SELECT
NM_019075.4:c.856-6163G>AMANE SELECT
NM_019076.5:c.856-6163G>AMANE SELECT
NM_019077.3:c.856-6163G>AMANE SELECT
NM_019078.2:c.868-6163G>AMANE SELECT
NM_019093.4:c.868-6163G>AMANE SELECT
NM_021027.3:c.856-6163G>AMANE SELECT
NM_205862.3:c.61-6163G>A
NP_000454.1:p.Arg195Lys
NP_000454.1:p.Arg195Lys
LRG_733t1:c.584G>A
LRG_733:g.5599G>A
LRG_733p1:p.Arg195Lys
NC_000002.11:g.234669517G>A
NC_000002.11:g.234669517G>A
NM_000463.2:c.584G>A

Protein change:

R195K

Links:

dbSNP: rs767764203

NCBI 1000 Genomes Browser:

rs767764203

Molecular consequence:

NM_001072.4:c.862-6163G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_007120.3:c.868-6163G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_019075.4:c.856-6163G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_019076.5:c.856-6163G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_019077.3:c.856-6163G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_019078.2:c.868-6163G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_019093.4:c.868-6163G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_021027.3:c.856-6163G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_205862.3:c.61-6163G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_000463.3:c.584G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Inborn genetic diseases
Identifiers:: MeSH: D030342; MedGen: C0950123

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003595469	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Dec 7, 2021)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003595469

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Dec 7, 2021)

germline

clinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV003595469.2

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

Description

The c.584G>A (p.R195K) alteration is located in exon 1 (coding exon 1) of the UGT1A1 gene. This alteration results from a G to A substitution at nucleotide position 584, causing the arginine (R) at amino acid position 195 to be replaced by a lysine (K). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	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: Oct 13, 2024

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