NM_001148.6(ANK2):c.2249A>G (p.Gln750Arg) AND Cardiovascular phenotype

Clinical significance:Likely benign (Last evaluated: Feb 22, 2019)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000621543.1

Allele description [Variation Report for NM_001148.6(ANK2):c.2249A>G (p.Gln750Arg)]

NM_001148.6(ANK2):c.2249A>G (p.Gln750Arg)

Gene:
ANK2:ankyrin 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
4q26
Genomic location:
Preferred name:
NM_001148.6(ANK2):c.2249A>G (p.Gln750Arg)
HGVS:
  • NC_000004.12:g.113288458A>G
  • NG_009006.2:g.475376A>G
  • NM_001127493.2:c.2186A>G
  • NM_001148.6:c.2249A>GMANE SELECT
  • NM_001354225.1:c.2249A>G
  • NM_001354228.1:c.2249A>G
  • NM_001354230.1:c.2294A>G
  • NM_001354231.1:c.2294A>G
  • NM_001354232.1:c.2249A>G
  • NM_001354235.1:c.2249A>G
  • NM_001354236.1:c.2249A>G
  • NM_001354237.1:c.2294A>G
  • NM_001354239.1:c.2186A>G
  • NM_001354240.1:c.2294A>G
  • NM_001354241.1:c.2294A>G
  • NM_001354242.1:c.2294A>G
  • NM_001354243.1:c.2186A>G
  • NM_001354244.1:c.2186A>G
  • NM_001354245.1:c.2150A>G
  • NM_001354246.1:c.2249A>G
  • NM_001354249.1:c.2162A>G
  • NM_001354252.1:c.2186A>G
  • NM_001354253.1:c.2087A>G
  • NM_001354254.1:c.2186A>G
  • NM_001354255.1:c.2186A>G
  • NM_001354256.1:c.2186A>G
  • NM_001354257.1:c.2087A>G
  • NM_001354258.1:c.2249A>G
  • NM_001354260.1:c.2063A>G
  • NM_001354261.1:c.2207A>G
  • NM_001354262.1:c.2186A>G
  • NM_001354264.1:c.2162A>G
  • NM_001354265.1:c.2249A>G
  • NM_001354266.1:c.2162A>G
  • NM_001354267.1:c.2162A>G
  • NM_001354268.1:c.2150A>G
  • NM_001354269.1:c.2039A>G
  • NM_001354270.1:c.2087A>G
  • NM_001354271.1:c.2063A>G
  • NM_001354272.1:c.2186A>G
  • NM_001354273.1:c.2051A>G
  • NM_001354274.1:c.2162A>G
  • NM_001354275.1:c.2186A>G
  • NM_001354276.1:c.2162A>G
  • NM_001354277.1:c.1964A>G
  • NM_020977.4:c.2249A>G
  • NP_001120965.1:p.Gln729Arg
  • NP_001139.3:p.Gln750Arg
  • NP_001341154.1:p.Gln750Arg
  • NP_001341157.1:p.Gln750Arg
  • NP_001341159.1:p.Gln765Arg
  • NP_001341160.1:p.Gln765Arg
  • NP_001341161.1:p.Gln750Arg
  • NP_001341164.1:p.Gln750Arg
  • NP_001341165.1:p.Gln750Arg
  • NP_001341166.1:p.Gln765Arg
  • NP_001341168.1:p.Gln729Arg
  • NP_001341169.1:p.Gln765Arg
  • NP_001341170.1:p.Gln765Arg
  • NP_001341171.1:p.Gln765Arg
  • NP_001341172.1:p.Gln729Arg
  • NP_001341173.1:p.Gln729Arg
  • NP_001341174.1:p.Gln717Arg
  • NP_001341175.1:p.Gln750Arg
  • NP_001341178.1:p.Gln721Arg
  • NP_001341181.1:p.Gln729Arg
  • NP_001341182.1:p.Gln696Arg
  • NP_001341183.1:p.Gln729Arg
  • NP_001341184.1:p.Gln729Arg
  • NP_001341185.1:p.Gln729Arg
  • NP_001341186.1:p.Gln696Arg
  • NP_001341187.1:p.Gln750Arg
  • NP_001341189.1:p.Gln688Arg
  • NP_001341190.1:p.Gln736Arg
  • NP_001341191.1:p.Gln729Arg
  • NP_001341193.1:p.Gln721Arg
  • NP_001341194.1:p.Gln750Arg
  • NP_001341195.1:p.Gln721Arg
  • NP_001341196.1:p.Gln721Arg
  • NP_001341197.1:p.Gln717Arg
  • NP_001341198.1:p.Gln680Arg
  • NP_001341199.1:p.Gln696Arg
  • NP_001341200.1:p.Gln688Arg
  • NP_001341201.1:p.Gln729Arg
  • NP_001341202.1:p.Gln684Arg
  • NP_001341203.1:p.Gln721Arg
  • NP_001341204.1:p.Gln729Arg
  • NP_001341205.1:p.Gln721Arg
  • NP_001341206.1:p.Gln655Arg
  • NP_066187.2:p.Gln750Arg
  • LRG_327t1:c.2249A>G
  • LRG_327:g.475376A>G
  • NC_000004.11:g.114209614A>G
  • NM_001148.4:c.2249A>G
Protein change:
Q655R
Links:
dbSNP: rs371787039
NCBI 1000 Genomes Browser:
rs371787039
Molecular consequence:
  • NM_001127493.2:c.2186A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001148.6:c.2249A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354225.1:c.2249A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354228.1:c.2249A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354230.1:c.2294A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354231.1:c.2294A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354232.1:c.2249A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354235.1:c.2249A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354236.1:c.2249A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354237.1:c.2294A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354239.1:c.2186A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354240.1:c.2294A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354241.1:c.2294A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354242.1:c.2294A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354243.1:c.2186A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354244.1:c.2186A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354245.1:c.2150A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354246.1:c.2249A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354249.1:c.2162A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354252.1:c.2186A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354253.1:c.2087A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354254.1:c.2186A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354255.1:c.2186A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354256.1:c.2186A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354257.1:c.2087A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354258.1:c.2249A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354260.1:c.2063A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354261.1:c.2207A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354262.1:c.2186A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354264.1:c.2162A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354265.1:c.2249A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354266.1:c.2162A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354267.1:c.2162A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354268.1:c.2150A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354269.1:c.2039A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354270.1:c.2087A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354271.1:c.2063A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354272.1:c.2186A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354273.1:c.2051A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354274.1:c.2162A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354275.1:c.2186A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354276.1:c.2162A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001354277.1:c.1964A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_020977.4:c.2249A>G - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Name:
Cardiovascular phenotype
Identifiers:
MedGen: CN230736

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000737892Ambry Geneticscriteria provided, single submitter
Likely benign
(Feb 22, 2019)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot provided1not providedclinical testing

Details of each submission

From Ambry Genetics, SCV000737892.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided

Description

Subpopulation frequency in support of benign classification

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknown1not providednot provided1not providednot providednot provided

Last Updated: May 23, 2021

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