rs12450628

Positions:

• chr17-37722426-C-T

Variant summary

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

The NM_000458.4(HNF1B):​c.1045+9169G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.285 in 152,078 control chromosomes in the GnomAD database, including 6,600 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 0.29 (6600 hom., cov: 32)
• Consequence: HNF1B NM_000458.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.154

Genes affected

HNF1B (HGNC:11630): (HNF1 homeobox B) This gene encodes a member of the homeodomain-containing superfamily of transcription factors. The protein binds to DNA as either a homodimer, or a heterodimer with the related protein hepatocyte nuclear factor 1-alpha. The gene has been shown to function in nephron development, and regulates development of the embryonic pancreas. Mutations in this gene result in renal cysts and diabetes syndrome and noninsulin-dependent diabetes mellitus, and expression of this gene is altered in some types of cancer. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]

LOC105371754 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.7).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.358 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
HNF1B	NM_000458.4	c.1045+9169G>A		intron_variant		ENST00000617811.5

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
HNF1B	ENST00000617811.5	c.1045+9169G>A		intron_variant		1	NM_000458.4
HNF1B	ENST00000613727.4	c.967+9169G>A		intron_variant		1
HNF1B	ENST00000621123.4	c.967+9169G>A		intron_variant		1		P1
HNF1B	ENST00000614313.4	c.1045+9169G>A		intron_variant		5

Frequencies

GnomAD3 genomes AF: 0.285 AC: 43382 AN: 151960 Hom.: 6592 Cov.: 32

Gnomad AFR AF: 0.179

Gnomad AMI AF: 0.418

Gnomad AMR AF: 0.342

Gnomad ASJ AF: 0.293

Gnomad EAS AF: 0.372

Gnomad SAS AF: 0.355

Gnomad FIN AF: 0.284

Gnomad MID AF: 0.323

Gnomad NFE AF: 0.323

Gnomad OTH AF: 0.319

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

GnomAD4 genome AF: 0.285 AC: 43394 AN: 152078 Hom.: 6600 Cov.: 32 AF XY: 0.287 AC XY: 21311 AN XY: 74332

Gnomad4 AFR AF: 0.178

Gnomad4 AMR AF: 0.343

Gnomad4 ASJ AF: 0.293

Gnomad4 EAS AF: 0.372

Gnomad4 SAS AF: 0.354

Gnomad4 FIN AF: 0.284

Gnomad4 NFE AF: 0.323

Gnomad4 OTH AF: 0.316

Alfa AF: 0.313 Hom.: 2554

Bravo AF: 0.284

Asia WGS AF: 0.344 AC: 1198 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.70
CADD	Benign	6.4
DANN	Benign	0.80

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: rs12450628; hg19: chr17-36082421;