NM_138352.3(SAMD1):c.99G>C (p.Glu33Asp) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Feb 3, 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:: RCV004124729.1

Allele description [Variation Report for NM_138352.3(SAMD1):c.99G>C (p.Glu33Asp)]

NM_138352.3(SAMD1):c.99G>C (p.Glu33Asp)

Genes:

LOC130063760:ATAC-STARR-seq lymphoblastoid silent region 10229 [Gene]
SAMD1:sterile alpha motif domain containing 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.12

Genomic location:

Preferred name:

NM_138352.3(SAMD1):c.99G>C (p.Glu33Asp)

HGVS:

NC_000019.10:g.14090322C>G
NG_029699.1:g.32426G>C
NM_138352.3:c.99G>CMANE SELECT
NP_612361.1:p.Glu33Asp
NC_000019.9:g.14201134C>G
NM_138352.1:c.99G>C

Protein change:

E33D

Molecular consequence:

NM_138352.3:c.99G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

Recent activity

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maturase K (chloroplast) [Eperua rubiginosa var. rubiginosa]
maturase K (chloroplast) [Eperua rubiginosa var. rubiginosa]
gi|2594663546|gb|WOG35086.1|

Protein
Uncultured Caloramator sp. clone TERI PRE JH1 B87 16S ribosomal RNA gene, partia...
Uncultured Caloramator sp. clone TERI PRE JH1 B87 16S ribosomal RNA gene, partial sequence
gi|1477051518|gb|MG001873.1|

Nucleotide
Uncultured bacterium clone TERI PRE JH1 B90 16S ribosomal RNA gene, partial sequ...
Uncultured bacterium clone TERI PRE JH1 B90 16S ribosomal RNA gene, partial sequence
gi|1477051521|gb|MG001876.1|

Nucleotide
Sylvioidea NADH dehydrogenase subunit 2 (ND2) gene, complete cds; mitochondrial.
Sylvioidea NADH dehydrogenase subunit 2 (ND2) gene, complete cds; mitochondrial.
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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003610626	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Feb 3, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003610626

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Feb 3, 2022)

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, SCV003610626.2

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

Description

The c.99G>C (p.E33D) alteration is located in exon (coding exon ) of the SAMD1 gene. This alteration results from a G to C substitution at nucleotide position 99, causing the glutamic acid (E) at amino acid position 33 to be replaced by an aspartic acid (D). 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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