NM_002454.3(MTRR):c.1761T>C (p.Tyr587=) AND not provided

Germline classification:: Benign (2 submissions)
Last evaluated:: Sep 13, 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:: RCV001812073.17

Allele description [Variation Report for NM_002454.3(MTRR):c.1761T>C (p.Tyr587=)]

NM_002454.3(MTRR):c.1761T>C (p.Tyr587=)

Gene:

MTRR:5-methyltetrahydrofolate-homocysteine methyltransferase reductase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

5p15.31

Genomic location:

Preferred name:

NM_002454.3(MTRR):c.1761T>C (p.Tyr587=)

Other names:

p.Y614Y:TAT>TAC

HGVS:

NC_000005.10:g.7896948T>C
NG_008856.1:g.32845T>C
NM_001364440.2:c.1761T>C
NM_001364441.2:c.1761T>C
NM_001364442.2:c.1761T>C
NM_002454.3:c.1761T>CMANE SELECT
NM_024010.4:c.1761T>C
NP_001351369.1:p.Tyr587=
NP_001351370.1:p.Tyr587=
NP_001351371.1:p.Tyr587=
NP_002445.2:p.Tyr587=
NP_076915.3:p.Tyr587=
NC_000005.9:g.7897061T>C
NM_002454.2:c.1761T>C
NM_024010.2:c.1842T>C
NR_134480.2:n.1840T>C
NR_134481.2:n.1765T>C
NR_134482.2:n.1700T>C
NR_157168.2:n.1814T>C
NR_157169.2:n.1674T>C
NR_157170.2:n.1840T>C
NR_157171.2:n.1697T>C
NR_157172.2:n.1611T>C
NR_157173.2:n.1851T>C
NR_157174.2:n.1852T>C
NR_157175.2:n.2006T>C
NR_157176.2:n.2169T>C
NR_157177.2:n.1849T>C
NR_157178.2:n.1877T>C

Links:

dbSNP: rs6874544

NCBI 1000 Genomes Browser:

rs6874544

Molecular consequence:

NR_134480.2:n.1840T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_134481.2:n.1765T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_134482.2:n.1700T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_157168.2:n.1814T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_157169.2:n.1674T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_157170.2:n.1840T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_157171.2:n.1697T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_157172.2:n.1611T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_157173.2:n.1851T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_157174.2:n.1852T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_157175.2:n.2006T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_157176.2:n.2169T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_157177.2:n.1849T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NR_157178.2:n.1877T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NM_001364440.2:c.1761T>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001364441.2:c.1761T>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001364442.2:c.1761T>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_002454.3:c.1761T>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_024010.4:c.1761T>C - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Synonyms:: none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM
Identifiers:: MedGen: C3661900

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001474358	ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	criteria provided, single submitter (ARUP Molecular Germline Variant Investigation Process 2024)	Benign (Sep 13, 2023)	germline	clinical testing	Citation Link,
SCV005298625	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

SCV001474358

ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

criteria provided, single submitter

(ARUP Molecular Germline Variant Investigation Process 2024)

Benign
(Sep 13, 2023)

germline

clinical testing

Citation Link,

SCV005298625

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	not provided
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 ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories, SCV001474358.5

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

From Breakthrough Genomics, Breakthrough Genomics, SCV005298625.1

#	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: Feb 25, 2025

ClinVar

Relating variation to medicine