rs9289235

Variant names:

• chr3-124435313-G-C
• rs9289235
• NM_001388419.1:c.3048+788G>C

Your query was ambiguous. Multiple possible variants found:

• chr3-124435313-G-C
• chr3-124435313-G-T

Variant summary

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

The NM_001388419.1(KALRN):​c.3048+788G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.358 in 152,042 control chromosomes in the GnomAD database, including 9,964 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 0.36 (9964 hom., cov: 32)
• Consequence: KALRN NM_001388419.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.155
• Publications: 2 publications found

Genes affected

KALRN (HGNC:4814): (kalirin RhoGEF kinase) Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with the huntingtin-associated protein 1, which is a huntingtin binding protein that may function in vesicle trafficking. [provided by RefSeq, Apr 2016]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.498 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
KALRN	NM_001388419.1	c.3048+788G>C		intron_variant	Intron 17 of 59	ENST00000682506.1	NP_001375348.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
KALRN	ENST00000682506.1	c.3048+788G>C		intron_variant	Intron 17 of 59		NM_001388419.1	ENSP00000508359.1

Frequencies

GnomAD3 genomes AF: 0.358 AC: 54370 AN: 151924 Hom.: 9958 Cov.: 32

Gnomad AFR AF: 0.309

Gnomad AMI AF: 0.397

Gnomad AMR AF: 0.399

Gnomad ASJ AF: 0.332

Gnomad EAS AF: 0.514

Gnomad SAS AF: 0.469

Gnomad FIN AF: 0.374

Gnomad MID AF: 0.396

Gnomad NFE AF: 0.357

Gnomad OTH AF: 0.333

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

GnomAD4 genome AF: 0.358 AC: 54396 AN: 152042 Hom.: 9964 Cov.: 32 AF XY: 0.363 AC XY: 26953 AN XY: 74332

African (AFR) AF: 0.309 AC: 12805 AN: 41462

American (AMR) AF: 0.400 AC: 6103 AN: 15270

Ashkenazi Jewish (ASJ) AF: 0.332 AC: 1153 AN: 3470

East Asian (EAS) AF: 0.514 AC: 2655 AN: 5162

South Asian (SAS) AF: 0.468 AC: 2253 AN: 4812

European-Finnish (FIN) AF: 0.374 AC: 3959 AN: 10586

Middle Eastern (MID) AF: 0.384 AC: 113 AN: 294

European-Non Finnish (NFE) AF: 0.357 AC: 24289 AN: 67974

Other (OTH) AF: 0.335 AC: 704 AN: 2100

Alfa AF: 0.189 Hom.: 378

Bravo AF: 0.356

Asia WGS AF: 0.439 AC: 1530 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	4.4
DANN	Benign	0.37
PhyloP100		0.15
Mutation Taster		=100/0	polymorphism (auto)

Splicing

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

Other links and lift over

dbSNP: rs9289235; hg19: chr3-124154160;