NM_020975.6(RET):c.337+9G>A AND Pheochromocytoma

Germline classification:: Likely benign (1 submission)
Last evaluated:: Apr 27, 2017
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:: RCV000372689.13

Allele description [Variation Report for NM_020975.6(RET):c.337+9G>A]

NM_020975.6(RET):c.337+9G>A

Gene:

RET:ret proto-oncogene [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

10q11.21

Genomic location:

Preferred name:

NM_020975.6(RET):c.337+9G>A

HGVS:

NC_000010.11:g.43100731G>A
NG_007489.1:g.28663G>A
NM_001406743.1:c.337+9G>A
NM_001406744.1:c.337+9G>A
NM_001406759.1:c.337+9G>A
NM_001406760.1:c.337+9G>A
NM_001406761.1:c.337+9G>A
NM_001406762.1:c.337+9G>A
NM_001406763.1:c.337+9G>A
NM_001406764.1:c.337+9G>A
NM_001406765.1:c.337+9G>A
NM_001406766.1:c.337+9G>A
NM_001406767.1:c.337+9G>A
NM_001406768.1:c.337+9G>A
NM_001406769.1:c.337+9G>A
NM_001406770.1:c.337+9G>A
NM_001406771.1:c.337+9G>A
NM_001406772.1:c.337+9G>A
NM_001406773.1:c.337+9G>A
NM_001406774.1:c.337+9G>A
NM_001406775.1:c.337+9G>A
NM_001406776.1:c.337+9G>A
NM_001406777.1:c.337+9G>A
NM_001406778.1:c.337+9G>A
NM_001406779.1:c.337+9G>A
NM_001406780.1:c.337+9G>A
NM_001406781.1:c.337+9G>A
NM_001406782.1:c.337+9G>A
NM_001406783.1:c.337+9G>A
NM_001406784.1:c.74-8300G>A
NM_001406785.1:c.337+9G>A
NM_001406786.1:c.337+9G>A
NM_001406787.1:c.337+9G>A
NM_001406788.1:c.337+9G>A
NM_001406789.1:c.337+9G>A
NM_001406790.1:c.337+9G>A
NM_001406791.1:c.337+9G>A
NM_001406792.1:c.74-11368G>A
NM_001406793.1:c.74-11368G>A
NM_001406794.1:c.74-11368G>A
NM_020630.7:c.337+9G>A
NM_020975.6:c.337+9G>AMANE SELECT
LRG_518t1:c.337+9G>A
LRG_518:g.28663G>A
NC_000010.10:g.43596179G>A
NM_020975.4:c.337+9G>A
NM_020975.5:c.337+9G>A

Links:

dbSNP: rs2435351

NCBI 1000 Genomes Browser:

rs2435351

Molecular consequence:

NM_001406743.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406744.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406759.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406760.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406761.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406762.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406763.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406764.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406765.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406766.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406767.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406768.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406769.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406770.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406771.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406772.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406773.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406774.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406775.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406776.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406777.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406778.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406779.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406780.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406781.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406782.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406783.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406784.1:c.74-8300G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406785.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406786.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406787.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406788.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406789.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406790.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406791.1:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406792.1:c.74-11368G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406793.1:c.74-11368G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001406794.1:c.74-11368G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_020630.7:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_020975.6:c.337+9G>A - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:: Pheochromocytoma
Synonyms:: Chromaffinoma; Chromaffin paraganglioma; Chromaffin tumor; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0008233; MedGen: C0031511; Orphanet: 29072; OMIM: 171300; Human Phenotype Ontology: HP:0002666

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Human DNA sequence from clone RP11-631M21 on chromosome 10, complete sequence
Human DNA sequence from clone RP11-631M21 on chromosome 10, complete sequence
gi|22204440|emb|AL713922.12|

Nucleotide
Chromosome 20 open reading frame 30 [Homo sapiens]
Chromosome 20 open reading frame 30 [Homo sapiens]
gi|127799581|gb|AAI10409.2|

Protein
unnamed protein product [Homo sapiens]
unnamed protein product [Homo sapiens]
gi|189054991|dbj|BAG37975.1|

Protein
Caprella acanthifera voucher SFC8-002 cytochrome oxidase subunit 1 (COI) gene, p...
Caprella acanthifera voucher SFC8-002 cytochrome oxidase subunit 1 (COI) gene, partial cds; mitochondrial
gi|1104306666|gnl|uoguelph|FCCOM227 OI-5P|gb|KX223999.1|

Nucleotide
flavoprotein subunit of succinate dehydrogenase, partial [Toxoplasma gondii TgCa...
flavoprotein subunit of succinate dehydrogenase, partial [Toxoplasma gondii TgCatPRC2]
gi|1008950769|gb|KYK68078.1||gnl|WG P|cds.TGPRC2_215590A

Protein

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000362240	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification Criteria 13 December 2019)	Likely benign (Apr 27, 2017)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000362240

Illumina Laboratory Services, Illumina

criteria provided, single submitter

(ICSL Variant Classification Criteria 13 December 2019)

Likely benign
(Apr 27, 2017)

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 Illumina Laboratory Services, Illumina, SCV000362240.3

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

Description

This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases allowed determination this variant is unlikely to cause disease. Therefore, this variant is classified as likely benign.

#	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: Nov 10, 2024

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