Variant 16-82000830-C-G details in Genebe, Genetics Data Aggregator

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_StrongBA1

The ENST00000328945.7(SDR42E1):c.29G>C(p.Ser10Thr) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0277 in 1,612,950 control chromosomes in the GnomAD database, including 5,071 homozygotes. In-silico tool predicts a benign outcome for this variant. 15/20 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another nucleotide change resulting in same amino acid change has been previously reported as Likely benignin UniProt.

Frequency

Genomes: 𝑓 0.11 ( 2577 hom., cov: 32)

Exomes 𝑓: 0.020 ( 2494 hom. )

Consequence

SDR42E1
ENST00000328945.7 missense

Scores

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 0.528

Variant links:

Genes affected

SDR42E1 (HGNC:29834): (short chain dehydrogenase/reductase family 42E, member 1) Predicted to enable oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor. Predicted to be involved in steroid biosynthetic process. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

SDR42E1 links:

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ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -12 ACMG points.

BP4

Computational evidence support a benign effect (MetaRNN=0.0076619387).

BA1

GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.338 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein
SDR42E1	NM_145168.3 linkuse as main transcript	c.29G>C	p.Ser10Thr	missense_variant	2/3	ENST00000328945.7	NP_660151.2
SDR42E1	XM_005256257.5 linkuse as main transcript	c.29G>C	p.Ser10Thr	missense_variant	3/4		XP_005256314.1
SDR42E1	XM_011523471.4 linkuse as main transcript	c.-98G>C		5_prime_UTR_variant	1/3		XP_011521773.1
SDR42E1	XM_047434925.1 linkuse as main transcript	c.-95G>C		5_prime_UTR_variant	1/3		XP_047290881.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris
SDR42E1	ENST00000328945.7 linkuse as main transcript	c.29G>C	p.Ser10Thr	missense_variant	2/3	1	NM_145168.3	ENSP00000332407	P1
SDR42E1	ENST00000532128.5 linkuse as main transcript	c.-98G>C		5_prime_UTR_variant	2/4	5		ENSP00000434529
SDR42E1	ENST00000534209.1 linkuse as main transcript	n.362G>C		non_coding_transcript_exon_variant	3/4	2

Frequencies

GnomAD3 genomes

AF:

0.106

AC:

16107

AN:

152112

Hom.:

2558

Cov.:

show subpopulations

Gnomad AFR

AF:

0.343

Gnomad AMI

AF:

0.00

Gnomad AMR

AF:

0.0459

Gnomad ASJ

AF:

0.0135

Gnomad EAS

AF:

0.0429

Gnomad SAS

AF:

0.0728

Gnomad FIN

AF:

0.000283

Gnomad MID

AF:

0.0475

Gnomad NFE

AF:

0.00651

Gnomad OTH

AF:

0.0737

GnomAD3 exomes

AF:

0.0385

AC:

9574

AN:

248908

Hom.:

1042

AF XY:

0.0341

AC XY:

4604

AN XY:

135104

show subpopulations

Gnomad AFR exome

AF:

0.344

Gnomad AMR exome

AF:

0.0229

Gnomad ASJ exome

AF:

0.0113

Gnomad EAS exome

AF:

0.0391

Gnomad SAS exome

AF:

0.0574

Gnomad FIN exome

AF:

0.000698

Gnomad NFE exome

AF:

0.00671

Gnomad OTH exome

AF:

0.0262

GnomAD4 exome

AF:

0.0195

AC:

28489

AN:

1460720

Hom.:

2494

Cov.:

AF XY:

0.0196

AC XY:

14243

AN XY:

726704

show subpopulations

Gnomad4 AFR exome

AF:

0.349

Gnomad4 AMR exome

AF:

0.0262

Gnomad4 ASJ exome

AF:

0.0107

Gnomad4 EAS exome

AF:

0.0228

Gnomad4 SAS exome

AF:

0.0568

Gnomad4 FIN exome

AF:

0.000712

Gnomad4 NFE exome

AF:

0.00639

Gnomad4 OTH exome

AF:

0.0377

GnomAD4 genome

AF:

0.106

AC:

16165

AN:

152230

Hom.:

2577

Cov.:

AF XY:

0.104

AC XY:

7723

AN XY:

74442

show subpopulations

Gnomad4 AFR

AF:

0.343

Gnomad4 AMR

AF:

0.0458

Gnomad4 ASJ

AF:

0.0135

Gnomad4 EAS

AF:

0.0419

Gnomad4 SAS

AF:

0.0729

Gnomad4 FIN

AF:

0.000283

Gnomad4 NFE

AF:

0.00651

Gnomad4 OTH

AF:

0.0753

Alfa

AF:

0.0144

Hom.:

124

Bravo

AF:

0.118

TwinsUK

AF:

0.00782

AC:

ALSPAC

AF:

0.00519

AC:

ESP6500AA

AF:

0.325

AC:

1212

ESP6500EA

AF:

0.00829

AC:

ExAC

AF:

0.0450

AC:

5438

Asia WGS

AF:

0.106

AC:

368

AN:

3478

EpiCase

AF:

0.00824

EpiControl

AF:

0.00830

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Benign

0.057

BayesDel_addAF

Benign

-0.63

BayesDel_noAF

Benign

-0.54

CADD

Benign

3.1

DANN

Benign

0.095

DEOGEN2

Benign

0.00040

Eigen

Benign

-1.2

Eigen_PC

Benign

-1.1

FATHMM_MKL

Benign

0.0042

LIST_S2

Benign

0.039

MetaRNN

Benign

0.0077

MetaSVM

Benign

-1.1

MutationAssessor

Benign

-0.96

MutationTaster

Benign

1.0

PrimateAI

Benign

0.36

PROVEAN

Benign

0.42

REVEL

Benign

0.13

Sift

Benign

1.0

Sift4G

Benign

0.67

Polyphen

0.0

Vest4

0.025

MPC

0.010

ClinPred

0.00014

GERP RS

2.5

Varity_R

0.056

gMVP

0.42

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

Below is the list of publications found by LitVar. It may be empty.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Computational scores

Splicing

Publications

LitVar

Other links and lift over