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. Variant got 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

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

Verdict is Uncertain_significance. Variant got 0 ACMG points.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CSRP3-AS1	NR_183675.1	n.207+13585_207+13593delTTTTTTTTT		intron_variant	Intron 1 of 5

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CSRP3	ENST00000533783.2	c.-170_-162delAAAAAAAAA		5_prime_UTR_variant	Exon 1 of 7	1		ENSP00000431813.1
CSRP3-AS1	ENST00000527978.1	n.145+13585_145+13593delTTTTTTTTT		intron_variant	Intron 1 of 3	5

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

Gnomad4 NFE exome AF: 0.00

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

Gnomad4 AFR AF: 0.0000336

Gnomad4 AMR AF: 0.00

Gnomad4 ASJ AF: 0.00

Gnomad4 EAS AF: 0.00

Gnomad4 SAS AF: 0.00

Gnomad4 FIN AF: 0.00

Gnomad4 NFE AF: 0.00

Gnomad4 OTH AF: 0.00

Bravo AF: 0.0000113

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs34865888; hg19: chr11-19232040;