rs4821536

Variant names:

• chr22-36813403-C-A
• rs4821536
• NM_001315532.2:c.304+243G>T

Your query was ambiguous. Multiple possible variants found:

• chr22-36813403-C-A
• chr22-36813403-C-G
• chr22-36813403-C-T

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_001315532.2(PVALB):​c.304+243G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. 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: not found (cov: 30)
  • Exomes 𝑓: 0.0 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: PVALB NM_001315532.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.94
• Publications: 4 publications found

Genes affected

PVALB (HGNC:9704): (parvalbumin) The protein encoded by this gene is a high affinity calcium ion-binding protein that is structurally and functionally similar to calmodulin and troponin C. The encoded protein is thought to be involved in muscle relaxation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001315532.2. 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
	PVALB	NM_001315532.2	MANE Select	c.304+243G>T		intron	N/A	NP_001302461.1	P20472
	PVALB	NM_002854.3		c.304+243G>T		intron	N/A	NP_002845.1	P20472

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PVALB	ENST00000417718.7	TSL:1 MANE Select	c.304+243G>T		intron	N/A	ENSP00000400247.2	P20472
	PVALB	ENST00000216200.9	TSL:1	c.304+243G>T		intron	N/A	ENSP00000216200.5	P20472
	PVALB	ENST00000912200.1		c.304+243G>T		intron	N/A	ENSP00000582259.1

Frequencies

GnomAD3 genomes Cov.: 30

GnomAD4 exome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0 AN: 323688 Hom.: 0 Cov.: 3 AF XY: 0.00 AC XY: 0 AN XY: 167430

African (AFR) AF: 0.00 AC: 0 AN: 10222

American (AMR) AF: 0.00 AC: 0 AN: 14326

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 10412

East Asian (EAS) AF: 0.00 AC: 0 AN: 25426

South Asian (SAS) AF: 0.00 AC: 0 AN: 21314

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 21882

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 1796

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 198464

Other (OTH) AF: 0.00 AC: 0 AN: 19846

GnomAD4 genome Cov.: 30

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	0.13
DANN	Benign	0.19
PhyloP100		-1.9

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		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: rs4821536; hg19: chr22-37209447;