rs368480650

Variant names:

• chr19-13212219-G-A
• rs368480650
• NM_001127222.2:c.6190-3C>T

Your query was ambiguous. Multiple possible variants found:

• chr19-13212219-G-A
• chr19-13212219-G-T

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_001127222.2(CACNA1A):​c.6190-3C>T variant causes a splice region, intron change. The variant allele was found at a frequency of 0.00000657 in 152,238 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. 3/3 splice prediction tools predict no significant impact on normal splicing. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.0000066 (0 hom., cov: 34)
• Consequence: CACNA1A NM_001127222.2 splice_region, intron
• Scores: Splicing: ADA: 0.001602
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 5.99

Genes affected

CACNA1A (HGNC:1388): (calcium voltage-gated channel subunit alpha1 A) Voltage-dependent calcium channels mediate the entry of calcium ions into excitable cells, and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, and gene expression. Calcium channels are multisubunit complexes composed of alpha-1, beta, alpha-2/delta, and gamma subunits. The channel activity is directed by the pore-forming alpha-1 subunit, whereas, the others act as auxiliary subunits regulating this activity. The distinctive properties of the calcium channel types are related primarily to the expression of a variety of alpha-1 isoforms, alpha-1A, B, C, D, E, and S. This gene encodes the alpha-1A subunit, which is predominantly expressed in neuronal tissue. Mutations in this gene are associated with 2 neurologic disorders, familial hemiplegic migraine and episodic ataxia 2. This gene also exhibits polymorphic variation due to (CAG)n-repeats. Multiple transcript variants encoding different isoforms have been found for this gene. In one set of transcript variants, the (CAG)n-repeats occur in the 3' UTR, and are not associated with any disease. But in another set of variants, an insertion extends the coding region to include the (CAG)n-repeats which encode a polyglutamine tract. Expansion of the (CAG)n-repeats from the normal 4-18 to 21-33 in the coding region is associated with spinocerebellar ataxia 6. [provided by RefSeq, Jul 2016]

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.41).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CACNA1A	NM_001127222.2	c.6190-3C>T		splice_region_variant, intron_variant	Intron 42 of 46	ENST00000360228.11	NP_001120694.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CACNA1A	ENST00000360228.11	c.6190-3C>T		splice_region_variant, intron_variant	Intron 42 of 46	1	NM_001127222.2	ENSP00000353362.5
CACNA1A	ENST00000638029.1	c.6208-3C>T		splice_region_variant, intron_variant	Intron 43 of 47	5		ENSP00000489829.1
CACNA1A	ENST00000573710.7	c.6196-3C>T		splice_region_variant, intron_variant	Intron 42 of 46	5		ENSP00000460092.3
CACNA1A	ENST00000635727.1	c.6193-3C>T		splice_region_variant, intron_variant	Intron 42 of 46	5		ENSP00000490001.1
CACNA1A	ENST00000637769.1	c.6193-3C>T		splice_region_variant, intron_variant	Intron 42 of 46	1		ENSP00000489778.1
CACNA1A	ENST00000636012.1	c.6193-3C>T		splice_region_variant, intron_variant	Intron 42 of 45	5		ENSP00000490223.1
CACNA1A	ENST00000637736.1	c.6052-3C>T		splice_region_variant, intron_variant	Intron 41 of 45	5		ENSP00000489861.1
CACNA1A	ENST00000636389.1	c.6193-3C>T		splice_region_variant, intron_variant	Intron 42 of 46	5		ENSP00000489992.1
CACNA1A	ENST00000637432.1	c.6208-3C>T		splice_region_variant, intron_variant	Intron 43 of 47	5		ENSP00000490617.1
CACNA1A	ENST00000636549.1	c.6199-3C>T		splice_region_variant, intron_variant	Intron 43 of 47	5		ENSP00000490578.1
CACNA1A	ENST00000637927.1	c.6196-3C>T		splice_region_variant, intron_variant	Intron 42 of 46	5		ENSP00000489715.1
CACNA1A	ENST00000635895.1	c.6193-3C>T		splice_region_variant, intron_variant	Intron 42 of 46	5		ENSP00000490323.1
CACNA1A	ENST00000638009.2	c.6193-3C>T		splice_region_variant, intron_variant	Intron 42 of 46	1		ENSP00000489913.1
CACNA1A	ENST00000637276.1	c.6193-3C>T		splice_region_variant, intron_variant	Intron 42 of 45	5		ENSP00000489777.1
CACNA1A	ENST00000636768.1	n.*492-3C>T		splice_region_variant, intron_variant	Intron 7 of 9	5		ENSP00000490190.2

Frequencies

GnomAD3 genomes AF: 0.00000657 AC: 1 AN: 152238 Hom.: 0 Cov.: 34

Gnomad AFR AF: 0.00

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.00

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00

Gnomad FIN AF: 0.0000941

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.00

Gnomad OTH AF: 0.00

GnomAD4 exome Cov.: 31

GnomAD4 genome AF: 0.00000657 AC: 1 AN: 152238 Hom.: 0 Cov.: 34 AF XY: 0.0000134 AC XY: 1 AN XY: 74378

Gnomad4 AFR AF: 0.00

Gnomad4 AMR AF: 0.00

Gnomad4 ASJ AF: 0.00

Gnomad4 EAS AF: 0.00

Gnomad4 SAS AF: 0.00

Gnomad4 FIN AF: 0.0000941

Gnomad4 NFE AF: 0.00

Gnomad4 OTH AF: 0.00

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.41
CADD	Benign	15
DANN	Benign	0.90

Splicing

Name	Calibrated prediction	Score	Prediction
dbscSNV1_ADA	Benign	0.0016
dbscSNV1_RF	Benign	0.11
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: rs368480650; hg19: chr19-13323033;