NM_182608.4(ANKRD33):c.40G>C (p.Gly14Arg) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 6, 2023
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:: RCV004327326.1

Allele description [Variation Report for NM_182608.4(ANKRD33):c.40G>C (p.Gly14Arg)]

NM_182608.4(ANKRD33):c.40G>C (p.Gly14Arg)

Gene:

ANKRD33:ankyrin repeat domain 33 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

12q13.13

Genomic location:

Preferred name:

NM_182608.4(ANKRD33):c.40G>C (p.Gly14Arg)

HGVS:

NC_000012.12:g.51888226G>C
NM_001130015.2:c.-362G>C
NM_001304459.2:c.-362G>C
NM_001304460.2:c.-443G>C
NM_182608.4:c.40G>CMANE SELECT
NP_872414.3:p.Gly14Arg
NC_000012.11:g.52282010G>C
NM_182608.3:c.40G>C

Protein change:

G14R

Molecular consequence:

NM_001130015.2:c.-362G>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001304459.2:c.-362G>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001304460.2:c.-443G>C - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_182608.4:c.40G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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PREDICTED: Homo sapiens methyltransferase like 26 (METTL26), transcript variant ...
PREDICTED: Homo sapiens methyltransferase like 26 (METTL26), transcript variant X1, mRNA
gi|2462551312|ref|XM_054314189.1|

Nucleotide
Phytophthora cytochrome oxidase subunit I gene, partial cds; mitochondrial.
Phytophthora cytochrome oxidase subunit I gene, partial cds; mitochondrial.
PopSet: 507480174

PopSet
Phytophthora internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA...
Phytophthora internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene, complete sequence; and internal transcribed spacer 2, partial sequence.
PopSet: 507480234

PopSet
LOC105960275 [Erythranthe guttata]
LOC105960275 [Erythranthe guttata]
Gene ID:105960275

Gene
LOC105960125 [Erythranthe guttata]
LOC105960125 [Erythranthe guttata]
Gene ID:105960125

Gene

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003987688	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jun 6, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003987688

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jun 6, 2023)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV003987688.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

The c.40G>C (p.G14R) alteration is located in exon 1 (coding exon 1) of the ANKRD33 gene. This alteration results from a G to C substitution at nucleotide position 40, causing the glycine (G) at amino acid position 14 to be replaced by an arginine (R). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 10, 2024

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