rs75609241

Variant names:

• chr8-29224768-G-A
• rs75609241
• NM_015254.4:c.149+20578C>T

Your query was ambiguous. Multiple possible variants found:

• chr8-29224768-G-A
• chr8-29224768-G-C

Variant summary

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

The NM_015254.4(KIF13B):​c.149+20578C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0212 in 152,106 control chromosomes in the GnomAD database, including 74 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 0.021 (74 hom., cov: 32)
• Consequence: KIF13B NM_015254.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.500
• Publications: 2 publications found

Genes affected

KIF13B (HGNC:14405): (kinesin family member 13B) Enables 14-3-3 protein binding activity and protein kinase binding activity. Involved in regulation of axonogenesis. Located in axon and cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.0551 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
KIF13B	NM_015254.4	c.149+20578C>T		intron_variant	Intron 2 of 39	ENST00000524189.6	NP_056069.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
KIF13B	ENST00000524189.6	c.149+20578C>T		intron_variant	Intron 2 of 39	1	NM_015254.4	ENSP00000427900.1

Frequencies

GnomAD3 genomes AF: 0.0212 AC: 3223 AN: 151988 Hom.: 74 Cov.: 32

Gnomad AFR AF: 0.00467

Gnomad AMI AF: 0.0219

Gnomad AMR AF: 0.00912

Gnomad ASJ AF: 0.0513

Gnomad EAS AF: 0.000577

Gnomad SAS AF: 0.0610

Gnomad FIN AF: 0.0690

Gnomad MID AF: 0.0191

Gnomad NFE AF: 0.0239

Gnomad OTH AF: 0.0158

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

GnomAD4 genome AF: 0.0212 AC: 3222 AN: 152106 Hom.: 74 Cov.: 32 AF XY: 0.0232 AC XY: 1726 AN XY: 74350

African (AFR) AF: 0.00465 AC: 193 AN: 41484

American (AMR) AF: 0.00910 AC: 139 AN: 15268

Ashkenazi Jewish (ASJ) AF: 0.0513 AC: 178 AN: 3468

East Asian (EAS) AF: 0.000578 AC: 3 AN: 5186

South Asian (SAS) AF: 0.0609 AC: 293 AN: 4814

European-Finnish (FIN) AF: 0.0690 AC: 729 AN: 10560

Middle Eastern (MID) AF: 0.0205 AC: 6 AN: 292

European-Non Finnish (NFE) AF: 0.0239 AC: 1628 AN: 68010

Other (OTH) AF: 0.0156 AC: 33 AN: 2112

Alfa AF: 0.0177 Hom.: 16

Bravo AF: 0.0154

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	1.1
DANN	Benign	0.63
PhyloP100		-0.50
Mutation Taster		=100/0	polymorphism

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: rs75609241; hg19: chr8-29082285;