NM_001201543.2(FAM161A):c.1057_1058del (p.Asn353fs) AND Retinitis pigmentosa 28

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: May 14, 2023
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:: RCV003460121.1

Allele description [Variation Report for NM_001201543.2(FAM161A):c.1057_1058del (p.Asn353fs)]

NM_001201543.2(FAM161A):c.1057_1058del (p.Asn353fs)

Gene:

FAM161A:FAM161 centrosomal protein A [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

2p15

Genomic location:

Preferred name:

NM_001201543.2(FAM161A):c.1057_1058del (p.Asn353fs)

HGVS:

NC_000002.12:g.61839947_61839948del
NG_028125.1:g.19197_19198del
NG_028125.2:g.19113_19114del
NM_001201543.1:c.1057_1058del
NM_001201543.2:c.1057_1058delMANE SELECT
NM_032180.3:c.1057_1058del
NP_001188472.1:p.Asn353fs
NP_115556.2:p.Asn353fs
NC_000002.11:g.62067082_62067083del
NR_037710.2:n.1020_1021del

Protein change:

N353fs

Molecular consequence:

NM_001201543.2:c.1057_1058del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_032180.3:c.1057_1058del - frameshift variant - [Sequence Ontology: SO:0001589]
NR_037710.2:n.1020_1021del - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:: Retinitis pigmentosa 28 (RP28)
Synonyms:: RP 28
Identifiers:: MONDO: MONDO:0011630; MedGen: C1419614; Orphanet: 791; OMIM: 606068

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004195955	Baylor Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely pathogenic (May 14, 2023)	unknown	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004195955

Baylor Genetics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely pathogenic
(May 14, 2023)

unknown

clinical testing

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	unknown	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 Baylor Genetics, SCV004195955.1

#	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: Dec 30, 2023

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