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NM_001148.6(ANK2):c.7183A>C (p.Thr2395Pro) AND Cardiovascular phenotype

Germline classification:
Likely benign (1 submission)
Last evaluated:
Jun 8, 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:
RCV002377012.2

Allele description [Variation Report for NM_001148.6(ANK2):c.7183A>C (p.Thr2395Pro)]

NM_001148.6(ANK2):c.7183A>C (p.Thr2395Pro)

Genes:
LOC126807137:CDK7 strongly-dependent group 2 enhancer GRCh37_chr4:114276560-114277759 [Gene]
ANK2:ankyrin 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
4q26
Genomic location:
Preferred name:
NM_001148.6(ANK2):c.7183A>C (p.Thr2395Pro)
HGVS:
  • NC_000004.12:g.113355801A>C
  • NG_009006.2:g.542719A>C
  • NM_001127493.3:c.4400-5022A>C
  • NM_001148.6:c.7183A>CMANE SELECT
  • NM_001354225.2:c.4439-5022A>C
  • NM_001354228.2:c.4328-5022A>C
  • NM_001354230.2:c.4406-5022A>C
  • NM_001354231.2:c.4469-5022A>C
  • NM_001354232.2:c.4463-5022A>C
  • NM_001354235.2:c.4424-5022A>C
  • NM_001354236.2:c.4325-5022A>C
  • NM_001354237.2:c.4505-5022A>C
  • NM_001354239.2:c.4397-5022A>C
  • NM_001354240.2:c.4472-5022A>C
  • NM_001354241.2:c.4472-5022A>C
  • NM_001354242.2:c.4469-5022A>C
  • NM_001354243.2:c.4364-5022A>C
  • NM_001354244.2:c.4361-5022A>C
  • NM_001354245.2:c.4265-5022A>C
  • NM_001354246.2:c.4424-5022A>C
  • NM_001354249.2:c.4241-5022A>C
  • NM_001354252.2:c.4397-5022A>C
  • NM_001354253.2:c.4202-5022A>C
  • NM_001354254.2:c.4376-5022A>C
  • NM_001354255.2:c.4364-5022A>C
  • NM_001354256.2:c.4361-5022A>C
  • NM_001354257.2:c.4166-5022A>C
  • NM_001354258.2:c.4328-5022A>C
  • NM_001354260.2:c.4142-5022A>C
  • NM_001354261.2:c.4286-5022A>C
  • NM_001354262.2:c.4265-5022A>C
  • NM_001354264.2:c.4262-5022A>C
  • NM_001354265.2:c.4424-5022A>C
  • NM_001354266.2:c.4241-5022A>C
  • NM_001354267.2:c.4241-5022A>C
  • NM_001354268.2:c.4229-5022A>C
  • NM_001354269.3:c.4214-5022A>C
  • NM_001354270.2:c.4202-5022A>C
  • NM_001354271.2:c.4142-5022A>C
  • NM_001354272.2:c.4298-5022A>C
  • NM_001354273.2:c.4127-5022A>C
  • NM_001354274.2:c.4193-5022A>C
  • NM_001354275.2:c.4265-5022A>C
  • NM_001354276.2:c.4241-5022A>C
  • NM_001354277.2:c.4043-5022A>C
  • NM_001354278.2:c.1955-5022A>C
  • NM_001354279.2:c.1991-5022A>C
  • NM_001354280.2:c.1976-5022A>C
  • NM_001354281.2:c.1955-5022A>C
  • NM_001354282.2:c.1991-5022A>C
  • NM_001386142.1:c.6949A>C
  • NM_001386143.1:c.4364-5022A>C
  • NM_001386144.1:c.4472-5022A>C
  • NM_001386146.1:c.4208-5022A>C
  • NM_001386147.1:c.4253-5022A>C
  • NM_001386148.2:c.4412-5022A>C
  • NM_001386149.1:c.4208-5022A>C
  • NM_001386150.1:c.4208-5022A>C
  • NM_001386151.1:c.4142-5022A>C
  • NM_001386152.1:c.4484-5022A>C
  • NM_001386153.1:c.4208-5022A>C
  • NM_001386154.1:c.4193-5022A>C
  • NM_001386156.1:c.4166-5022A>C
  • NM_001386157.1:c.4043-5022A>C
  • NM_001386158.1:c.3944-5022A>C
  • NM_001386160.1:c.4271-5022A>C
  • NM_001386161.1:c.4361-5022A>C
  • NM_001386162.1:c.4241-5022A>C
  • NM_001386166.1:c.3583A>C
  • NM_001386167.1:c.827-5022A>C
  • NM_001386174.1:c.7324A>C
  • NM_001386175.1:c.7300A>C
  • NM_001386186.2:c.4412-5022A>C
  • NM_001386187.2:c.4292-5022A>C
  • NM_020977.5:c.4427-5022A>C
  • NP_001139.3:p.Thr2395Pro
  • NP_001373071.1:p.Thr2317Pro
  • NP_001373095.1:p.Thr1195Pro
  • NP_001373103.1:p.Thr2442Pro
  • NP_001373104.1:p.Thr2434Pro
  • LRG_327t1:c.7183A>C
  • LRG_327:g.542719A>C
  • NC_000004.11:g.114276957A>C
  • NM_001148.4:c.7183A>C
  • NM_001148.5:c.7183A>C
Protein change:
T1195P
Links:
dbSNP: rs201693280
NCBI 1000 Genomes Browser:
rs201693280
Molecular consequence:
  • NM_001127493.3:c.4400-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354225.2:c.4439-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354228.2:c.4328-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354230.2:c.4406-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354231.2:c.4469-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354232.2:c.4463-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354235.2:c.4424-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354236.2:c.4325-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354237.2:c.4505-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354239.2:c.4397-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354240.2:c.4472-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354241.2:c.4472-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354242.2:c.4469-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354243.2:c.4364-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354244.2:c.4361-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354245.2:c.4265-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354246.2:c.4424-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354249.2:c.4241-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354252.2:c.4397-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354253.2:c.4202-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354254.2:c.4376-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354255.2:c.4364-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354256.2:c.4361-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354257.2:c.4166-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354258.2:c.4328-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354260.2:c.4142-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354261.2:c.4286-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354262.2:c.4265-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354264.2:c.4262-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354265.2:c.4424-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354266.2:c.4241-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354267.2:c.4241-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354268.2:c.4229-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354269.3:c.4214-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354270.2:c.4202-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354271.2:c.4142-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354272.2:c.4298-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354273.2:c.4127-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354274.2:c.4193-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354275.2:c.4265-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354276.2:c.4241-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354277.2:c.4043-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354278.2:c.1955-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354279.2:c.1991-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354280.2:c.1976-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354281.2:c.1955-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001354282.2:c.1991-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386143.1:c.4364-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386144.1:c.4472-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386146.1:c.4208-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386147.1:c.4253-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386148.2:c.4412-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386149.1:c.4208-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386150.1:c.4208-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386151.1:c.4142-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386152.1:c.4484-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386153.1:c.4208-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386154.1:c.4193-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386156.1:c.4166-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386157.1:c.4043-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386158.1:c.3944-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386160.1:c.4271-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386161.1:c.4361-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386162.1:c.4241-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386167.1:c.827-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386186.2:c.4412-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001386187.2:c.4292-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_020977.5:c.4427-5022A>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001148.6:c.7183A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001386142.1:c.6949A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001386166.1:c.3583A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001386174.1:c.7324A>C - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001386175.1:c.7300A>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Cardiovascular phenotype
Identifiers:
MedGen: CN230736

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002667138Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(Jun 8, 2022) 		germlineclinical testing

PubMed (6)
[See all records that cite these PMIDs]

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders.

Brion M, Blanco-Verea A, Sobrino B, Santori M, Gil R, Ramos-Luis E, Martinez M, Amigo J, Carracedo A.

Electrophoresis. 2014 Nov;35(21-22):3111-6. doi: 10.1002/elps.201400148. Epub 2014 Aug 6.

PubMed [citation]
PMID:
24981977

Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy.

Lopes LR, Syrris P, Guttmann OP, O'Mahony C, Tang HC, Dalageorgou C, Jenkins S, Hubank M, Monserrat L, McKenna WJ, Plagnol V, Elliott PM.

Heart. 2015 Feb;101(4):294-301. doi: 10.1136/heartjnl-2014-306387. Epub 2014 Oct 28.

PubMed [citation]
PMID:
25351510
PMCID:
PMC4345808
See all PubMed Citations (6)

Details of each submission

From Ambry Genetics, SCV002667138.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (6)

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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

Last Updated: Sep 29, 2024