rs4147358

Variant names:

• chr15-67135676-C-A
• rs4147358
• NM_005902.4:c.207-29219C>A

Your query was ambiguous. Multiple possible variants found:

• chr15-67135676-C-A
• chr15-67135676-C-G
• chr15-67135676-C-T

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_005902.4(SMAD3):​c.207-29219C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.309 in 151,928 control chromosomes in the GnomAD database, including 8,109 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.31 (8109 hom., cov: 31)
• Consequence: SMAD3 NM_005902.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.00500
• Publications: 17 publications found

Genes affected

SMAD3 (HGNC:6769): (SMAD family member 3) The SMAD family of proteins are a group of intracellular signal transducer proteins similar to the gene products of the Drosophila gene 'mothers against decapentaplegic' (Mad) and the C. elegans gene Sma. The SMAD3 protein functions in the transforming growth factor-beta signaling pathway, and transmits signals from the cell surface to the nucleus, regulating gene activity and cell proliferation. This protein forms a complex with other SMAD proteins and binds DNA, functioning both as a transcription factor and tumor suppressor. Mutations in this gene are associated with aneurysms-osteoarthritis syndrome and Loeys-Dietz Syndrome 3. [provided by RefSeq, May 2022]

SMAD3 Gene-Disease associations (from GenCC):

• aneurysm-osteoarthritis syndrome

  Inheritance: AD, Unknown Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Genomics England PanelApp, Orphanet, ClinGen, Labcorp Genetics (formerly Invitae), G2P
• familial thoracic aortic aneurysm and aortic dissection

  Inheritance: AD, Unknown Classification: DEFINITIVE, SUPPORTIVE Submitted by: Orphanet, ClinGen

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.78).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.584 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_005902.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SMAD3	NM_005902.4	MANE Select	c.207-29219C>A		intron	N/A	NP_005893.1	P84022-1
	SMAD3	NM_001407011.1		c.207-29219C>A		intron	N/A	NP_001393940.1	H3BQ00
	SMAD3	NM_001407012.1		c.207-29219C>A		intron	N/A	NP_001393941.1	A0AAQ5BHI7

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SMAD3	ENST00000327367.9	TSL:1 MANE Select	c.207-29219C>A		intron	N/A	ENSP00000332973.4	P84022-1
	SMAD3	ENST00000540846.6	TSL:1	c.-110+9692C>A		intron	N/A	ENSP00000437757.2	P84022-3
	SMAD3	ENST00000560424.2	TSL:3	c.207-29219C>A		intron	N/A	ENSP00000455540.2	H3BQ00

Frequencies

GnomAD3 genomes AF: 0.309 AC: 46917 AN: 151810 Hom.: 8095 Cov.: 31

Gnomad AFR AF: 0.413

Gnomad AMI AF: 0.208

Gnomad AMR AF: 0.358

Gnomad ASJ AF: 0.335

Gnomad EAS AF: 0.602

Gnomad SAS AF: 0.434

Gnomad FIN AF: 0.172

Gnomad MID AF: 0.313

Gnomad NFE AF: 0.224

Gnomad OTH AF: 0.329

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.309 AC: 46973 AN: 151928 Hom.: 8109 Cov.: 31 AF XY: 0.312 AC XY: 23142 AN XY: 74234

African (AFR) AF: 0.413 AC: 17100 AN: 41394

American (AMR) AF: 0.359 AC: 5480 AN: 15264

Ashkenazi Jewish (ASJ) AF: 0.335 AC: 1162 AN: 3464

East Asian (EAS) AF: 0.602 AC: 3113 AN: 5174

South Asian (SAS) AF: 0.434 AC: 2091 AN: 4822

European-Finnish (FIN) AF: 0.172 AC: 1810 AN: 10520

Middle Eastern (MID) AF: 0.316 AC: 93 AN: 294

European-Non Finnish (NFE) AF: 0.224 AC: 15245 AN: 67978

Other (OTH) AF: 0.327 AC: 690 AN: 2108

Alfa AF: 0.261 Hom.: 19602

Bravo AF: 0.328

Asia WGS AF: 0.489 AC: 1698 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.78
CADD	Benign	8.3
DANN	Benign	0.57
PhyloP100		0.0050
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

Other links and lift over

dbSNP: rs4147358;

hg19: chr15-67428014;