rs868438023

Variant names:

• chr15-40382906-C-A
• rs868438023
• NM_033286.4:c.71C>A

Your query was ambiguous. Multiple possible variants found:

• chr15-40382906-C-A
• chr15-40382906-C-G
• chr15-40382906-C-T

Variant summary

Our verdict is Uncertain significance. The variant received 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_033286.4(KNSTRN):​c.71C>A​(p.Ser24Tyr) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000656 in 152,328 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. 15/22 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.0000066 (0 hom., cov: 33)
• Consequence: KNSTRN NM_033286.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.169
• Publications: 0 publications found

Genes affected

KNSTRN (HGNC:30767): (kinetochore localized astrin (SPAG5) binding protein) Enables microtubule plus-end binding activity and protein homodimerization activity. Involved in several processes, including cellular response to epidermal growth factor stimulus; mitotic sister chromatid segregation; and regulation of attachment of spindle microtubules to kinetochore. Located in several cellular components, including kinetochore; microtubule cytoskeleton; and ruffle. Implicated in actinic keratosis and skin squamous cell carcinoma. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.08082119).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_033286.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	KNSTRN	NM_033286.4	MANE Select	c.71C>A	p.Ser24Tyr	missense	Exon 1 of 9	NP_150628.3	Q9Y448-1
	KNSTRN	NM_001142761.1		c.71C>A	p.Ser24Tyr	missense	Exon 1 of 9	NP_001136233.1	Q9Y448-2
	KNSTRN	NM_001142762.1		c.71C>A	p.Ser24Tyr	missense	Exon 1 of 8	NP_001136234.1	Q9Y448-3

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	KNSTRN	ENST00000249776.13	TSL:1 MANE Select	c.71C>A	p.Ser24Tyr	missense	Exon 1 of 9	ENSP00000249776.8	Q9Y448-1
	KNSTRN	ENST00000416151.6	TSL:3	c.71C>A	p.Ser24Tyr	missense	Exon 1 of 9	ENSP00000391233.2	Q9Y448-2
	KNSTRN	ENST00000448395.6	TSL:2	c.71C>A	p.Ser24Tyr	missense	Exon 1 of 8	ENSP00000393001.2	Q9Y448-3

Frequencies

GnomAD3 genomes AF: 0.00000657 AC: 1 AN: 152210 Hom.: 0 Cov.: 33

Gnomad AFR AF: 0.00

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.00

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.000193

Gnomad SAS AF: 0.00

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.00

Gnomad OTH AF: 0.00

GnomAD4 exome Cov.: 31

GnomAD4 genome AF: 0.00000656 AC: 1 AN: 152328 Hom.: 0 Cov.: 33 AF XY: 0.00 AC XY: 0 AN XY: 74492

African (AFR) AF: 0.00 AC: 0 AN: 41576

American (AMR) AF: 0.00 AC: 0 AN: 15302

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 3472

East Asian (EAS) AF: 0.000193 AC: 1 AN: 5180

South Asian (SAS) AF: 0.00 AC: 0 AN: 4832

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 10622

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 294

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 68026

Other (OTH) AF: 0.00 AC: 0 AN: 2112

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.11
BayesDel_addAF	Benign	-0.20	T
BayesDel_noAF	Benign	-0.52
CADD	Benign	16
DANN	Uncertain	0.98
DEOGEN2	Benign	0.0030	T
Eigen	Benign	-0.78
Eigen_PC	Benign	-0.88
FATHMM_MKL	Benign	0.0034	N
LIST_S2	Benign	0.66	T
M_CAP	Benign	0.0098	T
MetaRNN	Benign	0.081	T
MetaSVM	Benign	-1.0	T
MutationAssessor	Benign	0.69	N
PhyloP100		-0.17
PrimateAI	Benign	0.30	T
PROVEAN	Benign	-1.6	N
REVEL	Benign	0.063
Sift	Uncertain	0.0050	D
Sift4G	Uncertain	0.014	D
Polyphen		0.70	P
Vest4		0.18
MutPred		0.23		Loss of disorder (P = 0.0126)
MVP		0.14
MPC		0.35
ClinPred		0.25	T
GERP RS		0.10
PromoterAI		0.073	Neutral
Varity_R		0.086
gMVP		0.050

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: rs868438023; hg19: chr15-40675107;