rs34865888

Variant names:

• chr11-19210493-CTTTTTTTTT-C
• rs34865888
• ENST00000533783.2:c.-170_-162delAAAAAAAAA

Your query was ambiguous. Multiple possible variants found:

• chr11-19210493-CTTTTTTTTT-C
• chr11-19210493-CTTTTTTTTT-CTTT
• chr11-19210493-CTTTTTTTTT-CTTTT
• chr11-19210493-CTTTTTTTTT-CTTTTT
• chr11-19210493-CTTTTTTTTT-CTTTTTT
• chr11-19210493-CTTTTTTTTT-CTTTTTTT
• chr11-19210493-CTTTTTTTTT-CTTTTTTTT
• chr11-19210493-CTTTTTTTTT-CTTTTTTTTTT
• chr11-19210493-CTTTTTTTTT-CTTTTTTTTTTT
• chr11-19210493-CTTTTTTTTT-CTTTTTTTTTTTT
• chr11-19210493-CTTTTTTTTT-CTTTTTTTTTTTTT
• chr11-19210493-CTTTTTTTTT-CTTTTTTTTTTTTTTTTT

Variant summary

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

The ENST00000533783.2(CSRP3):​c.-170_-162delAAAAAAAAA variant causes a 5 prime UTR change involving the alteration of a non-conserved nucleotide. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: 𝑓 0.000010 (0 hom., cov: 0)
  • Exomes 𝑓: 0.0 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: CSRP3 ENST00000533783.2 5_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.16
• Publications: 1 publications found

Genes affected

CSRP3 (HGNC:2472): (cysteine and glycine rich protein 3) This gene encodes a member of the CSRP family of LIM domain proteins, which may be involved in regulatory processes important for development and cellular differentiation. The LIM/double zinc-finger motif found in this protein is found in a group of proteins with critical functions in gene regulation, cell growth, and somatic differentiation. Mutations in this gene are thought to cause heritable forms of hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) in humans. Alternatively spliced transcript variants with different 5' UTR, but encoding the same protein, have been found for this gene. [provided by RefSeq, Jul 2008]

CSRP3-AS1 (HGNC:54183): (CSRP3 and E2F8 antisense RNA 1)

ACMG classification

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

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000533783.2. 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
	CSRP3-AS1	NR_183675.1		n.207+13585_207+13593delTTTTTTTTT		intron	N/A

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CSRP3	ENST00000533783.2	TSL:1	c.-170_-162delAAAAAAAAA		5_prime_UTR	Exon 1 of 7	ENSP00000431813.1	P50461-1
	CSRP3-AS1	ENST00000527978.2	TSL:5	n.145+13585_145+13593delTTTTTTTTT		intron	N/A
	CSRP3-AS1	ENST00000789312.1		n.106+579_106+587delTTTTTTTTT		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.0000101 AC: 1 AN: 99004 Hom.: 0 Cov.: 0

Gnomad AFR AF: 0.0000336

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: 0.00

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.00

Gnomad OTH AF: 0.00

GnomAD4 exome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0 AN: 16 Hom.: 0 AF XY: 0.00 AC XY: 0 AN XY: 10

African (AFR) AC: 0 AN: 0

American (AMR) AC: 0 AN: 0

Ashkenazi Jewish (ASJ) AC: 0 AN: 0

East Asian (EAS) AC: 0 AN: 0

South Asian (SAS) AC: 0 AN: 0

European-Finnish (FIN) AC: 0 AN: 0

Middle Eastern (MID) AC: 0 AN: 0

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 16

Other (OTH) AC: 0 AN: 0

GnomAD4 genome AF: 0.0000101 AC: 1 AN: 99004 Hom.: 0 Cov.: 0 AF XY: 0.0000214 AC XY: 1 AN XY: 46654

African (AFR) AF: 0.0000336 AC: 1 AN: 29772

American (AMR) AF: 0.00 AC: 0 AN: 8926

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 2442

East Asian (EAS) AF: 0.00 AC: 0 AN: 3480

South Asian (SAS) AF: 0.00 AC: 0 AN: 2816

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 4382

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 230

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 44982

Other (OTH) AF: 0.00 AC: 0 AN: 1334

Alfa AF: 0.00 Hom.: 800

Bravo AF: 0.0000113

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
PhyloP100		1.2

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs34865888; hg19: chr11-19232040;