NM_145257.5:c.368-6597C>T

Variant names:

• chr1-229333603-G-A
• rs163771
• NM_145257.5:c.368-6597C>T

Variant summary

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

The NM_145257.5(CCSAP):​c.368-6597C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.393 in 151,868 control chromosomes in the GnomAD database, including 12,038 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 0.39 (12038 hom., cov: 31)
• Consequence: CCSAP NM_145257.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.358
• Publications: 2 publications found

Genes affected

CCSAP (HGNC:29578): (centriole, cilia and spindle associated protein) Enables microtubule binding activity. Involved in mitotic spindle microtubule depolymerization and regulation of mitotic spindle assembly. Located in axon; ciliary transition zone; and cytoskeleton. [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 (AFR) allele frequency at 95% confidence interval = 0.47 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_145257.5. 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
	CCSAP	NM_145257.5	MANE Select	c.368-6597C>T		intron	N/A	NP_660300.3
	CCSAP	NM_001410936.1		c.26-6597C>T		intron	N/A	NP_001397865.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CCSAP	ENST00000284617.7	TSL:1 MANE Select	c.368-6597C>T		intron	N/A	ENSP00000284617.2
	CCSAP	ENST00000366687.5	TSL:1	c.368-6597C>T		intron	N/A	ENSP00000355648.1
	CCSAP	ENST00000483092.1	TSL:1	n.799-6045C>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.393 AC: 59607 AN: 151754 Hom.: 12010 Cov.: 31

Gnomad AFR AF: 0.474

Gnomad AMI AF: 0.490

Gnomad AMR AF: 0.334

Gnomad ASJ AF: 0.518

Gnomad EAS AF: 0.242

Gnomad SAS AF: 0.231

Gnomad FIN AF: 0.353

Gnomad MID AF: 0.339

Gnomad NFE AF: 0.378

Gnomad OTH AF: 0.374

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

GnomAD4 genome AF: 0.393 AC: 59681 AN: 151868 Hom.: 12038 Cov.: 31 AF XY: 0.384 AC XY: 28499 AN XY: 74206

African (AFR) AF: 0.475 AC: 19671 AN: 41402

American (AMR) AF: 0.334 AC: 5094 AN: 15264

Ashkenazi Jewish (ASJ) AF: 0.518 AC: 1796 AN: 3466

East Asian (EAS) AF: 0.243 AC: 1251 AN: 5152

South Asian (SAS) AF: 0.232 AC: 1115 AN: 4816

European-Finnish (FIN) AF: 0.353 AC: 3717 AN: 10518

Middle Eastern (MID) AF: 0.340 AC: 100 AN: 294

European-Non Finnish (NFE) AF: 0.378 AC: 25712 AN: 67942

Other (OTH) AF: 0.370 AC: 780 AN: 2106

Alfa AF: 0.388 Hom.: 19158

Bravo AF: 0.396

Asia WGS AF: 0.247 AC: 860 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	0.79
DANN	Benign	0.64
PhyloP100		0.36
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: rs163771; hg19: chr1-229469350;