chr14-103702041-C-T

Variant names:

• chr14-103702041-C-T
• rs12432907
• ENST00000348520.10:c.*842C>T

Variant summary

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

The ENST00000348520.10(KLC1):​c.*842C>T variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.244 in 152,138 control chromosomes in the GnomAD database, including 4,837 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 0.24 (4835 hom., cov: 32)
  • Exomes 𝑓: 0.17 (2 hom.)
• Consequence: KLC1 ENST00000348520.10 3_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.52
• Publications: 20 publications found

Genes affected

KLC1 (HGNC:6387): (kinesin light chain 1) Conventional kinesin is a tetrameric molecule composed of two heavy chains and two light chains, and transports various cargos along microtubules toward their plus ends. The heavy chains provide the motor activity, while the light chains bind to various cargos. This gene encodes a member of the kinesin light chain family. It associates with kinesin heavy chain through an N-terminal domain, and six tetratricopeptide repeat (TPR) motifs are thought to be involved in binding of cargos such as vesicles, mitochondria, and the Golgi complex. Thus, kinesin light chains function as adapter molecules and not motors per se. Although previously named "kinesin 2", this gene is not a member of the kinesin-2 / kinesin heavy chain subfamily of kinesin motor proteins. Extensive alternative splicing produces isoforms with different C-termini that are proposed to bind to different cargos; however, the full-length nature and/or biological validity of most of these variants have not been determined. [provided by RefSeq, Jul 2008]

XRCC3 (HGNC:12830): (X-ray repair cross complementing 3) This gene encodes a member of the RecA/Rad51-related protein family that participates in homologous recombination to maintain chromosome stability and repair DNA damage. This gene functionally complements Chinese hamster irs1SF, a repair-deficient mutant that exhibits hypersensitivity to a number of different DNA-damaging agents and is chromosomally unstable. A rare microsatellite polymorphism in this gene is associated with cancer in patients of varying radiosensitivity. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.476 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000348520.10. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	XRCC3	NM_005432.4	MANE Select	c.561+1132G>A		intron	N/A	NP_005423.1
	XRCC3	NM_001100118.2		c.561+1132G>A		intron	N/A	NP_001093588.1
	XRCC3	NM_001100119.2		c.561+1132G>A		intron	N/A	NP_001093589.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	KLC1	ENST00000348520.10	TSL:1	c.*842C>T		3_prime_UTR	Exon 15 of 15	ENSP00000341154.6
	XRCC3	ENST00000555055.6	TSL:1 MANE Select	c.561+1132G>A		intron	N/A	ENSP00000452598.1
	XRCC3	ENST00000352127.11	TSL:1	c.561+1132G>A		intron	N/A	ENSP00000343392.7

Frequencies

GnomAD3 genomes AF: 0.245 AC: 37155 AN: 151936 Hom.: 4828 Cov.: 32

Gnomad AFR AF: 0.257

Gnomad AMI AF: 0.174

Gnomad AMR AF: 0.311

Gnomad ASJ AF: 0.246

Gnomad EAS AF: 0.492

Gnomad SAS AF: 0.373

Gnomad FIN AF: 0.241

Gnomad MID AF: 0.237

Gnomad NFE AF: 0.195

Gnomad OTH AF: 0.259

GnomAD4 exome AF: 0.167 AC: 14 AN: 84 Hom.: 2 Cov.: 0 AF XY: 0.167 AC XY: 11 AN XY: 66

African (AFR) AF: 0.500 AC: 2 AN: 4

American (AMR) AC: 0 AN: 0

Ashkenazi Jewish (ASJ) AF: 0.500 AC: 1 AN: 2

East Asian (EAS) AF: 0.00 AC: 0 AN: 2

South Asian (SAS) AC: 0 AN: 0

European-Finnish (FIN) AF: 0.125 AC: 1 AN: 8

Middle Eastern (MID) AC: 0 AN: 0

European-Non Finnish (NFE) AF: 0.152 AC: 10 AN: 66

Other (OTH) AF: 0.00 AC: 0 AN: 2

GnomAD4 genome AF: 0.245 AC: 37180 AN: 152054 Hom.: 4835 Cov.: 32 AF XY: 0.253 AC XY: 18768 AN XY: 74322

African (AFR) AF: 0.257 AC: 10653 AN: 41466

American (AMR) AF: 0.311 AC: 4756 AN: 15296

Ashkenazi Jewish (ASJ) AF: 0.246 AC: 853 AN: 3468

East Asian (EAS) AF: 0.492 AC: 2538 AN: 5156

South Asian (SAS) AF: 0.372 AC: 1796 AN: 4830

European-Finnish (FIN) AF: 0.241 AC: 2547 AN: 10562

Middle Eastern (MID) AF: 0.228 AC: 67 AN: 294

European-Non Finnish (NFE) AF: 0.195 AC: 13258 AN: 67966

Other (OTH) AF: 0.263 AC: 554 AN: 2108

Alfa AF: 0.216 Hom.: 6453

Bravo AF: 0.250

Asia WGS AF: 0.436 AC: 1516 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	0.90
DANN	Benign	0.33
PhyloP100		-1.5
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: rs12432907; hg19: chr14-104168378;