NM_173630.4(RTTN):c.4889G>C (p.Arg1630Thr) AND Microcephalic primordial dwarfism due to RTTN deficiency

Germline classification:: Likely benign (1 submission)
Last evaluated:: Feb 14, 2022
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:: RCV002498530.1

Allele description [Variation Report for NM_173630.4(RTTN):c.4889G>C (p.Arg1630Thr)]

NM_173630.4(RTTN):c.4889G>C (p.Arg1630Thr)

Gene:

RTTN:rotatin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

18q22.2

Genomic location:

Preferred name:

NM_173630.4(RTTN):c.4889G>C (p.Arg1630Thr)

HGVS:

NC_000018.10:g.70059901C>G
NG_033104.1:g.150826G>C
NM_001318520.2:c.2153G>C
NM_173630.4:c.4889G>CMANE SELECT
NP_001305449.1:p.Arg718Thr
NP_775901.3:p.Arg1630Thr
NC_000018.9:g.67727137C>G
NM_173630.3:c.4889G>C

Protein change:

R1630T

Links:

dbSNP: rs182595458

NCBI 1000 Genomes Browser:

rs182595458

Molecular consequence:

NM_001318520.2:c.2153G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_173630.4:c.4889G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Microcephalic primordial dwarfism due to RTTN deficiency (MSSP)
Synonyms:: Microcephaly, short stature, and polymicrogyria with or without seizures; MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA
Identifiers:: MONDO: MONDO:0018764; MedGen: C3553831; OMIM: 614833

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002799300	Fulgent Genetics, Fulgent Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely benign (Feb 14, 2022)	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

SCV002799300

Fulgent Genetics, Fulgent Genetics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely benign
(Feb 14, 2022)

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 Fulgent Genetics, Fulgent Genetics, SCV002799300.1

#	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: Oct 13, 2024

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