chr6-150004176-A-G

Variant names:

• chr6-150004176-A-G
• rs9479373
• ENST00000533735.3:n.168+897T>C

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The ENST00000533735.3(RAET1K):​n.168+897T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0316 in 152,250 control chromosomes in the GnomAD database, including 225 homozygotes. 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: 𝑓 0.032 (225 hom., cov: 33)
• Consequence: RAET1K ENST00000533735.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.675
• Publications: 1 publications found

Genes affected

RAET1K (HGNC:):

RAET1K (HGNC:16797): (retinoic acid early transcript 1K (pseudogene))

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.107 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
RAET1K	NR_024045.2	n.132+897T>C		intron_variant	Intron 1 of 3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
RAET1K	ENST00000533735.3	n.168+897T>C		intron_variant	Intron 1 of 3	1
RAET1K	ENST00000403651.2	n.85+897T>C		intron_variant	Intron 1 of 3	6
RAET1K	ENST00000779702.1	n.132+897T>C		intron_variant	Intron 1 of 4
RAET1K	ENST00000779705.1	n.94+897T>C		intron_variant	Intron 1 of 2

Frequencies

GnomAD3 genomes AF: 0.0315 AC: 4793 AN: 152134 Hom.: 223 Cov.: 33

Gnomad AFR AF: 0.109

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.0118

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00104

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.0158

Gnomad NFE AF: 0.000338

Gnomad OTH AF: 0.0239

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

GnomAD4 genome AF: 0.0316 AC: 4818 AN: 152250 Hom.: 225 Cov.: 33 AF XY: 0.0307 AC XY: 2287 AN XY: 74450

African (AFR) AF: 0.110 AC: 4558 AN: 41502

American (AMR) AF: 0.0118 AC: 180 AN: 15308

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 3472

East Asian (EAS) AF: 0.00 AC: 0 AN: 5184

South Asian (SAS) AF: 0.000415 AC: 2 AN: 4822

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 10622

Middle Eastern (MID) AF: 0.0170 AC: 5 AN: 294

European-Non Finnish (NFE) AF: 0.000338 AC: 23 AN: 68024

Other (OTH) AF: 0.0237 AC: 50 AN: 2112

Alfa AF: 0.0247 Hom.: 21

Bravo AF: 0.0357

Asia WGS AF: 0.00953 AC: 33 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	0.39
DANN	Benign	0.44
PhyloP100		-0.68

Splicing

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

Other links and lift over

dbSNP: rs9479373; hg19: chr6-150325312;