rs3774895

Variant names:

• chr4-5885713-A-C
• rs3774895
• NM_001014809.3:c.381+6876T>G

Your query was ambiguous. Multiple possible variants found:

• chr4-5885713-A-C
• chr4-5885713-A-G
• chr4-5885713-A-T

Variant summary

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

The NM_001014809.3(CRMP1):​c.381+6876T>G 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: 32)
• Consequence: CRMP1 NM_001014809.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.00
• Publications: 4 publications found

Genes affected

CRMP1 (HGNC:2365): (collapsin response mediator protein 1) This gene encodes a member of a family of cytosolic phosphoproteins expressed exclusively in the nervous system. The encoded protein is thought to be a part of the semaphorin signal transduction pathway implicated in semaphorin-induced growth cone collapse during neural development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]

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=-0.93).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001014809.3. 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
	CRMP1	NM_001014809.3	MANE Select	c.381+6876T>G		intron	N/A	NP_001014809.1	Q14194-2
	CRMP1	NM_001313.5		c.39+2515T>G		intron	N/A	NP_001304.1	Q14194-1
	CRMP1	NM_001288661.2		c.33+3912T>G		intron	N/A	NP_001275590.1	E9PD68

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CRMP1	ENST00000324989.12	TSL:1 MANE Select	c.381+6876T>G		intron	N/A	ENSP00000321606.7	Q14194-2
	CRMP1	ENST00000397890.7	TSL:1	c.39+2515T>G		intron	N/A	ENSP00000380987.2	Q14194-1
	CRMP1	ENST00000512574.1	TSL:2	c.33+3912T>G		intron	N/A	ENSP00000425742.1	E9PD68

Frequencies

GnomAD3 genomes Cov.: 32

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

GnomAD4 genome Cov.: 32

Alfa AF: 0.00 Hom.: 1094

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	1.6
DANN	Benign	0.36
PhyloP100		-1.0

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

Other links and lift over

dbSNP: rs3774895; hg19: chr4-5887440;