chr12-25241845-C-T

Position:

• chr12-25241845-C-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_004985.5(KRAS):​c.111+3429G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.541 in 151,914 control chromosomes in the GnomAD database, including 23,247 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 0.54 (23247 hom., cov: 31)
• Consequence: KRAS NM_004985.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.277

Genes affected

KRAS (HGNC:6407): (KRAS proto-oncogene, GTPase) This gene, a Kirsten ras oncogene homolog from the mammalian ras gene family, encodes a protein that is a member of the small GTPase superfamily. A single amino acid substitution is responsible for an activating mutation. The transforming protein that results is implicated in various malignancies, including lung adenocarcinoma, mucinous adenoma, ductal carcinoma of the pancreas and colorectal carcinoma. Alternative splicing leads to variants encoding two isoforms that differ in the C-terminal region. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.83).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.777 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
KRAS	NM_004985.5	c.111+3429G>A		intron_variant		ENST00000311936.8	NP_004976.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
KRAS	ENST00000311936.8	c.111+3429G>A		intron_variant		1	NM_004985.5	ENSP00000308495.3

Frequencies

GnomAD3 genomes AF: 0.541 AC: 82084 AN: 151796 Hom.: 23239 Cov.: 31

Gnomad AFR AF: 0.354

Gnomad AMI AF: 0.504

Gnomad AMR AF: 0.566

Gnomad ASJ AF: 0.651

Gnomad EAS AF: 0.798

Gnomad SAS AF: 0.602

Gnomad FIN AF: 0.567

Gnomad MID AF: 0.544

Gnomad NFE AF: 0.615

Gnomad OTH AF: 0.567

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

GnomAD4 genome AF: 0.541 AC: 82120 AN: 151914 Hom.: 23247 Cov.: 31 AF XY: 0.542 AC XY: 40257 AN XY: 74234

Gnomad4 AFR AF: 0.354

Gnomad4 AMR AF: 0.566

Gnomad4 ASJ AF: 0.651

Gnomad4 EAS AF: 0.798

Gnomad4 SAS AF: 0.601

Gnomad4 FIN AF: 0.567

Gnomad4 NFE AF: 0.615

Gnomad4 OTH AF: 0.568

Alfa AF: 0.582 Hom.: 12571

Bravo AF: 0.533

Asia WGS AF: 0.668 AC: 2322 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.83
CADD	Benign	1.7
DANN	Benign	0.73

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: rs12813551; hg19: chr12-25394779;