rs3138144

chr12-55720985-G-Cchr12-55720985-G-T

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_002905.5(RDH5):c.-32-168G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.375 in 151,898 control chromosomes in the GnomAD database, including 12,398 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency: Genomes: 𝑓 0.38 (12398 hom., cov: 32)
• Consequence: RDH5 NM_002905.5 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: 0.193

Genes affected

RDH5 (HGNC:9940): (retinol dehydrogenase 5) This gene encodes an enzyme belonging to the short-chain dehydrogenases/reductases (SDR) family. This retinol dehydrogenase functions to catalyze the final step in the biosynthesis of 11-cis retinaldehyde, which is the universal chromophore of visual pigments. Mutations in this gene cause autosomal recessive fundus albipunctatus, a rare form of night blindness that is characterized by a delay in the regeneration of cone and rod photopigments. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring upstream BLOC1S1 (biogenesis of lysosomal organelles complex-1, subunit 1) gene. [provided by RefSeq, Dec 2010]

BLOC1S1-RDH5 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BP6: Variant 12-55720985-G-C is Benign according to our data. Variant chr12-55720985-G-C is described in ClinVar as [Benign]. Clinvar id is 1266740.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.536 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
RDH5	NM_002905.5	c.-32-168G>C		intron_variant		ENST00000257895.10
BLOC1S1-RDH5	NR_037658.1	n.370-704G>C		intron_variant, non_coding_transcript_variant
RDH5	NM_001199771.3	c.-37-163G>C		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
RDH5	ENST00000257895.10	c.-32-168G>C		intron_variant		1	NM_002905.5	P1

Frequencies

GnomAD3 genomes AF: 0.375 AC: 56962 AN: 151784 Hom.: 12400 Cov.: 32

Gnomad AFR AF: 0.142

Gnomad AMI AF: 0.551

Gnomad AMR AF: 0.403

Gnomad ASJ AF: 0.475

Gnomad EAS AF: 0.433

Gnomad SAS AF: 0.555

Gnomad FIN AF: 0.459

Gnomad MID AF: 0.465

Gnomad NFE AF: 0.472

Gnomad OTH AF: 0.399

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

GnomAD4 genome AF: 0.375 AC: 56962 AN: 151898 Hom.: 12398 Cov.: 32 AF XY: 0.376 AC XY: 27933 AN XY: 74242

Gnomad4 AFR AF: 0.142

Gnomad4 AMR AF: 0.403

Gnomad4 ASJ AF: 0.475

Gnomad4 EAS AF: 0.432

Gnomad4 SAS AF: 0.554

Gnomad4 FIN AF: 0.459

Gnomad4 NFE AF: 0.472

Gnomad4 OTH AF: 0.402

Alfa AF: 0.312 Hom.: 1048

Bravo AF: 0.357

Asia WGS AF: 0.452 AC: 1571 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Nov 05, 2018

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
Cadd	Benign	2.8
Dann	Benign	0.66

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

Publications

LitVar

Other links and lift over

dbSNP: rs3138144; hg19: chr12-56114769; COSMIC: COSV57676044; COSMIC: COSV57676044;