NM_001077365.2(POMT1):c.1126G>A (p.Gly376Arg) AND not specified

Clinical significance:Benign/Likely benign (Last evaluated: Jan 16, 2017)

Review status:2 stars out of maximum of 4 stars

criteria provided, multiple submitters, no conflicts

Based on:
2 submissions [Details]
Record status:
current
Accession:
RCV000376051.3

Allele description [Variation Report for NM_001077365.2(POMT1):c.1126G>A (p.Gly376Arg)]

NM_001077365.2(POMT1):c.1126G>A (p.Gly376Arg)

Gene:
POMT1:protein O-mannosyltransferase 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9q34.13
Genomic location:
Preferred name:
NM_001077365.2(POMT1):c.1126G>A (p.Gly376Arg)
HGVS:
  • NC_000009.12:g.131513282G>A
  • NG_008896.1:g.15381G>A
  • NM_001077365.2:c.1126G>AMANE SELECT
  • NM_001077366.2:c.964G>A
  • NM_001136113.2:c.1126G>A
  • NM_001136114.2:c.775G>A
  • NM_001353193.2:c.1192G>A
  • NM_001353194.2:c.964G>A
  • NM_001353195.2:c.775G>A
  • NM_001353196.2:c.1036G>A
  • NM_001353197.2:c.1030G>A
  • NM_001353198.2:c.1030G>A
  • NM_001353199.2:c.841G>A
  • NM_001353200.2:c.670G>A
  • NM_001374689.1:c.1114G>A
  • NM_001374690.1:c.1126G>A
  • NM_001374691.1:c.775G>A
  • NM_001374692.1:c.775G>A
  • NM_001374693.1:c.824+1815G>A
  • NM_001374695.1:c.736G>A
  • NM_007171.3:c.1192G>A
  • NM_007171.4:c.1192G>A
  • NP_001070833.1:p.Gly376Arg
  • NP_001070834.1:p.Gly322Arg
  • NP_001129585.1:p.Gly376Arg
  • NP_001129586.1:p.Gly259Arg
  • NP_001340122.2:p.Gly398Arg
  • NP_001340123.1:p.Gly322Arg
  • NP_001340124.1:p.Gly259Arg
  • NP_001340125.1:p.Gly346Arg
  • NP_001340126.2:p.Gly344Arg
  • NP_001340127.2:p.Gly344Arg
  • NP_001340128.2:p.Gly281Arg
  • NP_001340129.1:p.Gly224Arg
  • NP_001361618.1:p.Gly372Arg
  • NP_001361619.1:p.Gly376Arg
  • NP_001361620.1:p.Gly259Arg
  • NP_001361621.1:p.Gly259Arg
  • NP_001361624.1:p.Gly246Arg
  • NP_009102.3:p.Gly398Arg
  • NP_009102.4:p.Gly398Arg
  • LRG_842t1:c.1192G>A
  • LRG_842t2:c.1126G>A
  • LRG_842p1:p.Gly398Arg
  • LRG_842p2:p.Gly376Arg
  • NC_000009.11:g.134388669G>A
  • NR_148391.2:n.1160G>A
  • NR_148392.2:n.1378G>A
  • NR_148393.2:n.1160G>A
  • NR_148394.2:n.1053G>A
  • NR_148395.2:n.1312G>A
  • NR_148396.2:n.946G>A
  • NR_148397.2:n.1210G>A
  • NR_148398.2:n.1165G>A
  • NR_148399.2:n.1552G>A
  • NR_148400.2:n.1151G>A
Protein change:
G224R
Links:
dbSNP: rs146869947
NCBI 1000 Genomes Browser:
rs146869947
Molecular consequence:
  • NM_001374693.1:c.824+1815G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001077365.2:c.1126G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001077366.2:c.964G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001136113.2:c.1126G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001136114.2:c.775G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353193.2:c.1192G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353194.2:c.964G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353195.2:c.775G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353196.2:c.1036G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353197.2:c.1030G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353198.2:c.1030G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353199.2:c.841G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353200.2:c.670G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001374689.1:c.1114G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001374690.1:c.1126G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001374691.1:c.775G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001374692.1:c.775G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001374695.1:c.736G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007171.3:c.1192G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007171.4:c.1192G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_148391.2:n.1160G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_148392.2:n.1378G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_148393.2:n.1160G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_148394.2:n.1053G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_148395.2:n.1312G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_148396.2:n.946G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_148397.2:n.1210G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_148398.2:n.1165G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_148399.2:n.1552G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_148400.2:n.1151G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
Observations:
1

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000337908EGL Genetic Diagnostics, Eurofins Clinical Diagnosticscriteria provided, single submitter
Benign
(Dec 16, 2015)
germlineclinical testing

Citation Link,

SCV000524077GeneDxcriteria provided, single submitter
Likely benign
(Jan 16, 2017)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot providednot providednot providedclinical testing
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From EGL Genetic Diagnostics, Eurofins Clinical Diagnostics, SCV000337908.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot provided1not providednot providednot provided

From GeneDx, SCV000524077.4

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Jun 14, 2021

Support Center