14-62834639-T-C

Position:

• chr14-62834639-T-C

Variant summary

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

The NM_139318.5(KCNH5):​c.1569+15014A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.329 in 151,762 control chromosomes in the GnomAD database, including 9,056 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 0.33 (9056 hom., cov: 31)
• Consequence: KCNH5 NM_139318.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.217

Genes affected

KCNH5 (HGNC:6254): (potassium voltage-gated channel subfamily H member 5) This gene encodes a member of voltage-gated potassium channels. Members of this family have diverse functions, including regulating neurotransmitter and hormone release, cardiac function, and cell volume. This protein is an outward-rectifying, noninactivating channel. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.567 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
KCNH5	NM_139318.5	c.1569+15014A>G		intron_variant		ENST00000322893.12
KCNH5	NM_172375.3	c.1569+15014A>G		intron_variant
KCNH5	XM_047431275.1	c.1569+15014A>G		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
KCNH5	ENST00000322893.12	c.1569+15014A>G		intron_variant		1	NM_139318.5	P1
KCNH5	ENST00000420622.6	c.1569+15014A>G		intron_variant		1
KCNH5	ENST00000394968.2	c.1395+15014A>G		intron_variant		2

Frequencies

GnomAD3 genomes AF: 0.329 AC: 49888 AN: 151644 Hom.: 9064 Cov.: 31

Gnomad AFR AF: 0.189

Gnomad AMI AF: 0.469

Gnomad AMR AF: 0.280

Gnomad ASJ AF: 0.422

Gnomad EAS AF: 0.482

Gnomad SAS AF: 0.586

Gnomad FIN AF: 0.455

Gnomad MID AF: 0.436

Gnomad NFE AF: 0.368

Gnomad OTH AF: 0.346

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

GnomAD4 genome AF: 0.329 AC: 49878 AN: 151762 Hom.: 9056 Cov.: 31 AF XY: 0.336 AC XY: 24949 AN XY: 74160

Gnomad4 AFR AF: 0.189

Gnomad4 AMR AF: 0.279

Gnomad4 ASJ AF: 0.422

Gnomad4 EAS AF: 0.481

Gnomad4 SAS AF: 0.585

Gnomad4 FIN AF: 0.455

Gnomad4 NFE AF: 0.368

Gnomad4 OTH AF: 0.347

Alfa AF: 0.366 Hom.: 13786

Bravo AF: 0.304

Asia WGS AF: 0.471 AC: 1636 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	3.4
DANN	Benign	0.72

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: rs243149; hg19: chr14-63301357;