chr10-43408759-A-G

Position:

• chr10-43408759-A-G

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP4_Moderate BA1

The NM_001098205.2(HNRNPF):​c.-279T>C variant causes a 5 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.655 in 152,014 control chromosomes in the GnomAD database, including 34,294 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 0.65 (34282 hom., cov: 32)
  • Exomes 𝑓: 0.67 (12 hom.)
• Consequence: HNRNPF NM_001098205.2 5_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.80

Genes affected

HNRNPF (HGNC:5039): (heterogeneous nuclear ribonucleoprotein F) This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins that complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and regulate alternative splicing, polyadenylation, 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 has three repeats of quasi-RRM domains that bind to RNAs which have guanosine-rich sequences. This protein is very similar to the family member hnRPH. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -10 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.46).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.76 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
HNRNPF	NM_001098204.2	c.-247+372T>C		intron_variant		ENST00000682386.1	NP_001091674.1
HNRNPF	NM_001098205.2	c.-279T>C		5_prime_UTR_variant	1/4		NP_001091675.1
HNRNPF	NM_004966.4	c.-247+331T>C		intron_variant			NP_004957.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
HNRNPF	ENST00000682386.1	c.-247+372T>C		intron_variant			NM_001098204.2	ENSP00000507787.1
HNRNPF	ENST00000337970.7	c.-247+331T>C		intron_variant		1		ENSP00000338477.3
HNRNPF	ENST00000356053.7	c.-279T>C		5_prime_UTR_variant	1/4	2		ENSP00000348345.3

Frequencies

GnomAD3 genomes AF: 0.655 AC: 99455 AN: 151844 Hom.: 34273 Cov.: 32

Gnomad AFR AF: 0.416

Gnomad AMI AF: 0.770

Gnomad AMR AF: 0.715

Gnomad ASJ AF: 0.645

Gnomad EAS AF: 0.735

Gnomad SAS AF: 0.642

Gnomad FIN AF: 0.749

Gnomad MID AF: 0.677

Gnomad NFE AF: 0.765

Gnomad OTH AF: 0.692

GnomAD4 exome AF: 0.673 AC: 35 AN: 52 Hom.: 12 Cov.: 0 AF XY: 0.636 AC XY: 28 AN XY: 44

Gnomad4 AMR exome AF: 1.00

Gnomad4 SAS exome AF: 0.500

Gnomad4 FIN exome AF: 0.875

Gnomad4 NFE exome AF: 0.625

GnomAD4 genome AF: 0.655 AC: 99497 AN: 151962 Hom.: 34282 Cov.: 32 AF XY: 0.654 AC XY: 48603 AN XY: 74286

Gnomad4 AFR AF: 0.415

Gnomad4 AMR AF: 0.715

Gnomad4 ASJ AF: 0.645

Gnomad4 EAS AF: 0.734

Gnomad4 SAS AF: 0.643

Gnomad4 FIN AF: 0.749

Gnomad4 NFE AF: 0.765

Gnomad4 OTH AF: 0.693

Alfa AF: 0.709 Hom.: 9796

Bravo AF: 0.643

Asia WGS AF: 0.670 AC: 2332 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.46
CADD	Benign	16
DANN	Benign	0.72
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.0

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs1416226; hg19: chr10-43904207;