NM_000137.4(FAH):c.455G>A (p.Trp152Ter) AND Tyrosinemia type I

This record was updated by the submitter. Please see the current version.

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Mar 22, 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:: RCV000409617.1

Allele description

NM_000137.4(FAH):c.455G>A (p.Trp152Ter)

Gene:

FAH:fumarylacetoacetate hydrolase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

15q25.1

Genomic location:

Preferred name:

NM_000137.4(FAH):c.455G>A (p.Trp152Ter)

HGVS:

NC_000015.10:g.80162336G>A
NG_012833.1:g.14338G>A
NM_000137.4:c.455G>AMANE SELECT
NM_001374377.1:c.455G>A
NM_001374380.1:c.455G>A
NP_000128.1:p.Trp152Ter
NP_001361306.1:p.Trp152Ter
NP_001361309.1:p.Trp152Ter
NC_000015.9:g.80454678G>A
NM_000137.2:c.455G>A

Protein change:

W152*

Links:

dbSNP: rs1057516679

NCBI 1000 Genomes Browser:

rs1057516679

Molecular consequence:

NM_000137.4:c.455G>A - nonsense - [Sequence Ontology: SO:0001587]
NM_001374377.1:c.455G>A - nonsense - [Sequence Ontology: SO:0001587]
NM_001374380.1:c.455G>A - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

Name:: Tyrosinemia type I (TYRSN1)
Synonyms:: Tyrosinemia type 1; Hepatorenal tyrosinemia; FAH deficiency; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0010161; MedGen: C0268490; Orphanet: 882; OMIM: 276700

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000486055	Counsyl	criteria provided, single submitter (Counsyl Autosomal and X-linked Recessive Disease Classification criteria (2015))	Likely pathogenic (Mar 22, 2016)	unknown	clinical testing	PubMed (1) [See all records that cite this PMID] mdi-5618_320494_Counsyl Autosomal and X-linked Recessive Disease Classification criteria (2015).pdf Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000486055

Counsyl

criteria provided, single submitter

(Counsyl Autosomal and X-linked Recessive Disease Classification criteria (2015))

Likely pathogenic
(Mar 22, 2016)

unknown

clinical testing

PubMed (1)
[See all records that cite this PMID]

mdi-5618_320494_Counsyl Autosomal and X-linked Recessive Disease Classification criteria (2015).pdf

Citation Link

Help

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

Citations

PubMed

[Analysis of clinical data and genetic mutations in three Chinese patients with tyrosinemia type I].

Yang N, Han LS, Ye J, Qiu WJ, Zhang HW, Gong ZW, Zhang YF, Wang Y, Gu XF.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Dec;29(6):648-52. doi: 10.3760/cma.j.issn.1003-9406.2012.06.005. Chinese.

PubMed [citation]

PMID:: 23225041

Details of each submission

From Counsyl, SCV000486055.1

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

Last Updated: Feb 20, 2022

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