10-4991646-A-G

Position:

• chr10-4991646-A-G

Variant summary

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

The NM_001393392.1(AKR1C2):​c.929+185T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency: Genomes: 𝑓 0.23 (3240 hom., cov: 19)
• Consequence: AKR1C2 NM_001393392.1 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -0.606

Genes affected

AKR1C2 (HGNC:385): (aldo-keto reductase family 1 member C2) This gene encodes a member of the aldo/keto reductase superfamily, which consists of more than 40 known enzymes and proteins. These enzymes catalyze the conversion of aldehydes and ketones to their corresponding alcohols using NADH and/or NADPH as cofactors. The enzymes display overlapping but distinct substrate specificity. This enzyme binds bile acid with high affinity, and shows minimal 3-alpha-hydroxysteroid dehydrogenase activity. This gene shares high sequence identity with three other gene members and is clustered with those three genes at chromosome 10p15-p14. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.97).
• BP6: Variant 10-4991646-A-G is Benign according to our data. Variant chr10-4991646-A-G is described in ClinVar as [Benign]. Clinvar id is 1183519.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.293 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
AKR1C2	NM_001393392.1	c.929+185T>C		intron_variant		ENST00000380753.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
AKR1C2	ENST00000380753.9	c.929+185T>C		intron_variant		1	NM_001393392.1	P1
AKR1C2	ENST00000421196.7	c.851+185T>C		intron_variant		1
AKR1C2	ENST00000460124.5	n.2389+185T>C		intron_variant, non_coding_transcript_variant		5

Frequencies

GnomAD3 genomes AF: 0.233 AC: 30638 AN: 131352 Hom.: 3239 Cov.: 19

Gnomad AFR AF: 0.273

Gnomad AMI AF: 0.177

Gnomad AMR AF: 0.201

Gnomad ASJ AF: 0.353

Gnomad EAS AF: 0.306

Gnomad SAS AF: 0.153

Gnomad FIN AF: 0.178

Gnomad MID AF: 0.325

Gnomad NFE AF: 0.221

Gnomad OTH AF: 0.247

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

GnomAD4 genome AF: 0.233 AC: 30656 AN: 131430 Hom.: 3240 Cov.: 19 AF XY: 0.229 AC XY: 14556 AN XY: 63702

Gnomad4 AFR AF: 0.273

Gnomad4 AMR AF: 0.201

Gnomad4 ASJ AF: 0.353

Gnomad4 EAS AF: 0.306

Gnomad4 SAS AF: 0.152

Gnomad4 FIN AF: 0.178

Gnomad4 NFE AF: 0.221

Gnomad4 OTH AF: 0.249

Alfa AF: 0.221 Hom.: 348

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

Jul 09, 2018

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.97
CADD	Benign	2.1
DANN	Benign	0.42

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.040		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: rs199743770; hg19: chr10-5033838; COSMIC: COSV66334515; COSMIC: COSV66334515;