NM_203349.4:c.657-9783A>G

Variant names:

• chr15-48900594-T-C
• rs8023445
• NM_203349.4:c.657-9783A>G

Variant summary

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

The NM_203349.4(SHC4):​c.657-9783A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.151 in 151,992 control chromosomes in the GnomAD database, including 1,913 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 0.15 (1913 hom., cov: 31)
• Consequence: SHC4 NM_203349.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.01
• Publications: 22 publications found

Genes affected

SHC4 (HGNC:16743): (SHC adaptor protein 4) Predicted to enable receptor tyrosine kinase binding activity. Predicted to be involved in transmembrane receptor protein tyrosine kinase signaling pathway. Predicted to act upstream of or within several processes, including apoptotic process; positive regulation of cell population proliferation; and stem cell differentiation. Predicted to be located in postsynaptic membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.96).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.207 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_203349.4. 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
	SHC4	NM_203349.4	MANE Select	c.657-9783A>G		intron	N/A	NP_976224.3

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SHC4	ENST00000332408.9	TSL:1 MANE Select	c.657-9783A>G		intron	N/A	ENSP00000329668.4	Q6S5L8-1

Frequencies

GnomAD3 genomes AF: 0.150 AC: 22848 AN: 151884 Hom.: 1903 Cov.: 31

Gnomad AFR AF: 0.210

Gnomad AMI AF: 0.112

Gnomad AMR AF: 0.142

Gnomad ASJ AF: 0.0612

Gnomad EAS AF: 0.185

Gnomad SAS AF: 0.121

Gnomad FIN AF: 0.214

Gnomad MID AF: 0.0350

Gnomad NFE AF: 0.113

Gnomad OTH AF: 0.115

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

GnomAD4 genome AF: 0.151 AC: 22895 AN: 151992 Hom.: 1913 Cov.: 31 AF XY: 0.155 AC XY: 11532 AN XY: 74286

African (AFR) AF: 0.210 AC: 8712 AN: 41442

American (AMR) AF: 0.143 AC: 2181 AN: 15288

Ashkenazi Jewish (ASJ) AF: 0.0612 AC: 212 AN: 3466

East Asian (EAS) AF: 0.185 AC: 956 AN: 5162

South Asian (SAS) AF: 0.121 AC: 583 AN: 4812

European-Finnish (FIN) AF: 0.214 AC: 2250 AN: 10530

Middle Eastern (MID) AF: 0.0310 AC: 9 AN: 290

European-Non Finnish (NFE) AF: 0.113 AC: 7650 AN: 67982

Other (OTH) AF: 0.114 AC: 240 AN: 2108

Alfa AF: 0.123 Hom.: 3704

Bravo AF: 0.152

Asia WGS AF: 0.168 AC: 583 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.96
CADD	Benign	1.5
DANN	Benign	0.73
PhyloP100		-1.0
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

Other links and lift over

dbSNP: rs8023445; hg19: chr15-49192791;