NM_000463.3(UGT1A1):c.611T>C (p.Met204Thr) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Aug 3, 2023
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:: RCV003491828.2

Allele description [Variation Report for NM_000463.3(UGT1A1):c.611T>C (p.Met204Thr)]

NM_000463.3(UGT1A1):c.611T>C (p.Met204Thr)

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.611T>C (p.Met204Thr)

HGVS:

NC_000002.12:g.233760898T>C
NG_002601.2:g.176155T>C
NG_033238.1:g.5626T>C
NM_000463.3:c.611T>CMANE SELECT
NM_001072.4:c.862-6136T>CMANE SELECT
NM_007120.3:c.868-6136T>CMANE SELECT
NM_019075.4:c.856-6136T>CMANE SELECT
NM_019076.5:c.856-6136T>CMANE SELECT
NM_019077.3:c.856-6136T>CMANE SELECT
NM_019078.2:c.868-6136T>CMANE SELECT
NM_019093.4:c.868-6136T>CMANE SELECT
NM_021027.3:c.856-6136T>CMANE SELECT
NM_205862.3:c.61-6136T>C
NP_000454.1:p.Met204Thr
NP_000454.1:p.Met204Thr
LRG_733t1:c.611T>C
LRG_733:g.5626T>C
LRG_733p1:p.Met204Thr
NC_000002.11:g.234669544T>C
NM_000463.2:c.611T>C

Protein change:

M204T

Molecular consequence:

NM_001072.4:c.862-6136T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_007120.3:c.868-6136T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_019075.4:c.856-6136T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_019076.5:c.856-6136T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_019077.3:c.856-6136T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_019078.2:c.868-6136T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_019093.4:c.868-6136T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_021027.3:c.856-6136T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_205862.3:c.61-6136T>C - intron variant - [Sequence Ontology: SO:0001627]
NM_000463.3:c.611T>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
SCV004237487	Revvity Omics, Revvity	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Aug 3, 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

SCV004237487

Revvity Omics, Revvity

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Aug 3, 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	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

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 Revvity Omics, Revvity, SCV004237487.1

#	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: Sep 1, 2024

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