ENST00000438189.6:c.-112-1326T>A

Variant names:

• chr11-67454383-T-A
• rs1790761
• ENST00000438189.6:c.-112-1326T>A

Variant summary

Our verdict is Likely benign. Variant got -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The ENST00000438189.6(CABP4):​c.-112-1326T>A 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: 33)
• Consequence: CABP4 ENST00000438189.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.668

Genes affected

CABP4 (HGNC:1386): (calcium binding protein 4) This gene encodes a member of the CABP family of calcium binding protein characterized by four EF-hand motifs. Mutations in this gene are associated with congenital stationary night blindness type 2B. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]

ACMG classification

Verdict is Likely_benign. Variant got -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CABP4	XM_024448615.2	c.-1041T>A		5_prime_UTR_variant	Exon 2 of 7		XP_024304383.1
CABP4	NM_001300896.3	c.-112-1326T>A		intron_variant	Intron 1 of 6		NP_001287825.1
CABP4	NM_001379183.1	c.-387-1051T>A		intron_variant	Intron 3 of 8		NP_001366112.1
CABP4	XM_005274114.4	c.71-1051T>A		intron_variant	Intron 1 of 4		XP_005274171.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CABP4	ENST00000438189.6	c.-112-1326T>A		intron_variant	Intron 1 of 6	1		ENSP00000401555.2
CABP4	ENST00000538060.1	n.296-1051T>A		intron_variant	Intron 1 of 1	4
CABP4	ENST00000542025.2	n.408-1051T>A		intron_variant	Intron 1 of 1	5

Frequencies

GnomAD3 genomes Cov.: 33

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

GnomAD4 genome Cov.: 33

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	3.4
DANN	Benign	0.54

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs1790761; hg19: chr11-67221854;