rs8009894

chr14-21223318-G-Achr14-21223318-G-C

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_004500.4(HNRNPC):c.365+7001C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.344 in 151,924 control chromosomes in the GnomAD database, including 9,192 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 0.34 (9192 hom., cov: 31)
• Consequence: HNRNPC NM_004500.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.418

Genes affected

HNRNPC (HGNC:5035): (heterogeneous nuclear ribonucleoprotein C) This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene can act as a tetramer and is involved in the assembly of 40S hnRNP particles. Multiple transcript variants encoding at least two different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.98).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.382 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
HNRNPC	NM_004500.4	c.365+7001C>T		intron_variant		ENST00000553300.6

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
HNRNPC	ENST00000553300.6	c.365+7001C>T		intron_variant		1	NM_004500.4	P3

Frequencies

GnomAD3 genomes AF: 0.344 AC: 52205 AN: 151806 Hom.: 9171 Cov.: 31

Gnomad AFR AF: 0.337

Gnomad AMI AF: 0.343

Gnomad AMR AF: 0.391

Gnomad ASJ AF: 0.287

Gnomad EAS AF: 0.302

Gnomad SAS AF: 0.344

Gnomad FIN AF: 0.358

Gnomad MID AF: 0.316

Gnomad NFE AF: 0.342

Gnomad OTH AF: 0.319

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

GnomAD4 genome AF: 0.344 AC: 52260 AN: 151924 Hom.: 9192 Cov.: 31 AF XY: 0.347 AC XY: 25749 AN XY: 74256

Gnomad4 AFR AF: 0.338

Gnomad4 AMR AF: 0.391

Gnomad4 ASJ AF: 0.287

Gnomad4 EAS AF: 0.303

Gnomad4 SAS AF: 0.342

Gnomad4 FIN AF: 0.358

Gnomad4 NFE AF: 0.342

Gnomad4 OTH AF: 0.317

Alfa AF: 0.355 Hom.: 1661

Bravo AF: 0.344

Asia WGS AF: 0.348 AC: 1211 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.98
Cadd	Benign	3.0
Dann	Benign	0.30

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

Publications

LitVar

Other links and lift over

dbSNP: rs8009894; hg19: chr14-21691477;