21-42475614-T-G

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_080860.4(RSPH1):c.877+284A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.131 in 145,314 control chromosomes in the GnomAD database, including 1,447 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency: Genomes: 𝑓 0.13 (1447 hom., cov: 23)
• Consequence: RSPH1 NM_080860.4 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -0.0510

Genes affected

RSPH1 (HGNC:12371): (radial spoke head component 1) This gene encodes a male meiotic metaphase chromosome-associated acidic protein. This gene is expressed in tissues with motile cilia or flagella, including the trachea, lungs, airway brushings, and testes. Mutations in this gene result in primary ciliary dyskinesia-24. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2014]

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BP6: Variant 21-42475614-T-G is Benign according to our data. Variant chr21-42475614-T-G is described in ClinVar as [Benign]. Clinvar id is 1282349.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.17 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
RSPH1	NM_080860.4	c.877+284A>C		intron_variant		ENST00000291536.8
RSPH1	NM_001286506.2	c.763+284A>C		intron_variant
RSPH1	XM_005261208.3	c.670+284A>C		intron_variant
RSPH1	XM_011529786.2	c.805+284A>C		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
RSPH1	ENST00000291536.8	c.877+284A>C		intron_variant		1	NM_080860.4	P1
RSPH1	ENST00000398352.3	c.763+284A>C		intron_variant		5
RSPH1	ENST00000493019.1	n.2495+284A>C		intron_variant, non_coding_transcript_variant		2

Frequencies

GnomAD3 genomes AF: 0.131 AC: 19001 AN: 145284 Hom.: 1445 Cov.: 23

Gnomad AFR AF: 0.0680

Gnomad AMI AF: 0.0392

Gnomad AMR AF: 0.101

Gnomad ASJ AF: 0.166

Gnomad EAS AF: 0.148

Gnomad SAS AF: 0.102

Gnomad FIN AF: 0.143

Gnomad MID AF: 0.162

Gnomad NFE AF: 0.172

Gnomad OTH AF: 0.127

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

GnomAD4 genome AF: 0.131 AC: 19006 AN: 145314 Hom.: 1447 Cov.: 23 AF XY: 0.129 AC XY: 9028 AN XY: 70184

Gnomad4 AFR AF: 0.0679

Gnomad4 AMR AF: 0.101

Gnomad4 ASJ AF: 0.166

Gnomad4 EAS AF: 0.148

Gnomad4 SAS AF: 0.103

Gnomad4 FIN AF: 0.143

Gnomad4 NFE AF: 0.172

Gnomad4 OTH AF: 0.128

Alfa AF: 0.160 Hom.: 448

Bravo AF: 0.123

Asia WGS AF: 0.120 AC: 417 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Jan 16, 2019

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
Cadd	Benign	0.55
Dann	Benign	0.44

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

Publications

LitVar

Other links and lift over

dbSNP: rs4920112; hg19: chr21-43895724;