NM_032043.3(BRIP1):c.3411T>C (p.Tyr1137=) AND Ovarian neoplasm

Germline classification:: Benign (1 submission)
Last evaluated:: Jun 18, 2016
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:: RCV000411217.10

Allele description [Variation Report for NM_032043.3(BRIP1):c.3411T>C (p.Tyr1137=)]

NM_032043.3(BRIP1):c.3411T>C (p.Tyr1137=)

Gene:

BRIP1:BRCA1 interacting DNA helicase 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17q23.2

Genomic location:

Preferred name:

NM_032043.3(BRIP1):c.3411T>C (p.Tyr1137=)

Other names:

NP_114432.2:p.Tyr1137=

HGVS:

NC_000017.11:g.61683635A>G
NG_007409.2:g.184925T>C
NM_032043.3:c.3411T>CMANE SELECT
NP_114432.2:p.Tyr1137=
NP_114432.2:p.Tyr1137=
LRG_300t1:c.3411T>C
LRG_300:g.184925T>C
LRG_300p1:p.Tyr1137=
NC_000017.10:g.59760996A>G
NM_032043.2:c.3411T>C
p.Tyr1137Tyr
p.Y1137Y

Links:

dbSNP: rs4986763

NCBI 1000 Genomes Browser:

rs4986763

Molecular consequence:

NM_032043.3:c.3411T>C - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: Ovarian neoplasm
Synonyms:: Neoplasm of ovary; Ovarian tumor; Ovarian Neoplasms
Identifiers:: MONDO: MONDO:0021068; MeSH: D010051; MedGen: C0919267; Human Phenotype Ontology: HP:0100615

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Chain I, CH848.3.D0949.10.17chim.6R.DS.SOSIP.664_N133D_N138T gp120
Chain I, CH848.3.D0949.10.17chim.6R.DS.SOSIP.664_N133D_N138T gp120
gi|2491197872|pdb|8DTO|I

Protein

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000489874	Counsyl	criteria provided, single submitter (Counsyl Autosomal Dominant Disease Classification criteria (2015))	Benign (Jun 18, 2016)	unknown	clinical testing	Counsyl Autosomal Dominant Disease Classification criteria (2015) Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000489874

Counsyl

criteria provided, single submitter

(Counsyl Autosomal Dominant Disease Classification criteria (2015))

Benign
(Jun 18, 2016)

unknown

clinical testing

Counsyl Autosomal Dominant Disease Classification criteria (2015)

Citation Link

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Summary from all submissions

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

Details of each submission

From Counsyl, SCV000489874.2

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

Last Updated: Nov 10, 2024

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