NM_001201543.2(FAM161A):c.981del (p.Phe327fs) AND Retinitis pigmentosa 28

Germline classification:: Likely pathogenic (1 submission)
Last evaluated:: Nov 2, 2021
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:: RCV003468092.1

Allele description [Variation Report for NM_001201543.2(FAM161A):c.981del (p.Phe327fs)]

NM_001201543.2(FAM161A):c.981del (p.Phe327fs)

Gene:

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

Variant type:

Deletion

Cytogenetic location:

2p15

Genomic location:

Preferred name:

NM_001201543.2(FAM161A):c.981del (p.Phe327fs)

HGVS:

NC_000002.12:g.61840025del
NG_028125.1:g.19121del
NG_028125.2:g.19037del
NM_001201543.1:c.981del
NM_001201543.2:c.981delMANE SELECT
NM_032180.3:c.981del
NP_001188472.1:p.Phe327fs
NP_115556.2:p.Phe327fs
NC_000002.11:g.62067160del
NR_037710.2:n.944del

Protein change:

F327fs

Molecular consequence:

NM_001201543.2:c.981del - frameshift variant - [Sequence Ontology: SO:0001589]
NM_032180.3:c.981del - frameshift variant - [Sequence Ontology: SO:0001589]
NR_037710.2:n.944del - 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
SCV004195981	Baylor Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely pathogenic (Nov 2, 2021)	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

SCV004195981

Baylor Genetics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely pathogenic
(Nov 2, 2021)

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, SCV004195981.1

#	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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