NM_000277.3(PAH):c.353-22C>T AND not provided

Germline classification:: Benign (3 submissions)
Last evaluated:: Mar 3, 2015
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:: RCV000088901.3

Allele description [Variation Report for NM_000277.3(PAH):c.353-22C>T]

NM_000277.3(PAH):c.353-22C>T

Gene:

PAH:phenylalanine hydroxylase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

12q23.2

Genomic location:

Preferred name:

NM_000277.3(PAH):c.353-22C>T

HGVS:

NC_000012.12:g.102877572G>A
NG_008690.2:g.85839C>T
NM_000277.3:c.353-22C>TMANE SELECT
NM_001354304.2:c.353-22C>T
NC_000012.11:g.103271350G>A
NC_000012.11:g.103271350G>A
NM_000277.1:c.353-22C>T
NM_000277.3(PAH):c.353-22C>TMANE SELECT

Links:

dbSNP: rs2037639

NCBI 1000 Genomes Browser:

rs2037639

Molecular consequence:

NM_000277.3:c.353-22C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001354304.2:c.353-22C>T - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

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Human fusion protein mRNA, complete cds
Human fusion protein mRNA, complete cds
gi|189399|gb|M82829.1|HUMORFD

Nucleotide
Garra litanensis voucher COFAAEMMF-GL1039 cytochrome c oxidase subunit I (COX1) ...
Garra litanensis voucher COFAAEMMF-GL1039 cytochrome c oxidase subunit I (COX1) gene, partial cds; mitochondrial
gi|1898829294|gb|MT954940.1|

Nucleotide
Garra litanensis voucher NE-074 cytochrome c oxidase subunit I (COI) gene, parti...
Garra litanensis voucher NE-074 cytochrome c oxidase subunit I (COI) gene, partial cds; mitochondrial
gi|1402367348|gb|MG736476.1|

Nucleotide
Garra litanensis isolate 14_2 cytochrome oxidase subunit I (COI) gene, partial c...
Garra litanensis isolate 14_2 cytochrome oxidase subunit I (COI) gene, partial cds; mitochondrial
gi|1678479042|gb|MK714218.1|

Nucleotide
Garra litanensis voucher NBFGRMU 8218E 16S ribosomal RNA gene, partial sequence;...
Garra litanensis voucher NBFGRMU 8218E 16S ribosomal RNA gene, partial sequence; mitochondrial
gi|1042420162|gb|KT878108.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000119499	DeBelle Laboratory for Biochemical Genetics, MUHC/MCH RESEARCH INSTITUTE	no classification provided	not provided	not provided	not provided
SCV001915541	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Benign (Mar 3, 2015)	germline	clinical testing	Citation Link,
SCV005235507	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

SCV000119499

DeBelle Laboratory for Biochemical Genetics, MUHC/MCH RESEARCH INSTITUTE

no classification provided

not provided

SCV001915541

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Benign
(Mar 3, 2015)

germline

clinical testing

Citation Link,

SCV005235507

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	clinical testing, not provided
not provided	not provided	not provided	not provided	not provided	not provided	1	not provided	literature only

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 DeBelle Laboratory for Biochemical Genetics, MUHC/MCH RESEARCH INSTITUTE, SCV000119499.1

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

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	not provided	not provided	1	not provided	not provided		not provided	not provided	not provided	not provided

From GeneDx, SCV001915541.1

#	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	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From Breakthrough Genomics, Breakthrough Genomics, SCV005235507.1

#	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: Sep 29, 2024

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