rs627297

Variant names:

• chr11-78052743-T-A
• rs627297
• ENST00000530054.1:c.310+20255A>T

Your query was ambiguous. Multiple possible variants found:

• chr11-78052743-T-A
• chr11-78052743-T-C
• chr11-78052743-T-G

Variant summary

Our verdict is Likely benign. The variant received -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_001203260.2(NDUFC2-KCTD14):​c.311-13985A>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. 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: not found (cov: 32)
• Consequence: NDUFC2-KCTD14 NM_001203260.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.396
• Publications: 11 publications found

Genes affected

NDUFC2-KCTD14 (HGNC:42956): (NDUFC2-KCTD14 readthrough) This locus represents naturally occurring read-through transcription between the neighboring NDUFC2 (NADH dehydrogenase (ubiquinone) 1, subcomplex unknown, 2, 14.5kDa) and KCTD14 (potassium channel tetramerisation domain containing 14) genes on chromosome 11. The read-through transcripts share sequence identity with the upstream gene product and one variant has a frameshifted C-terminal region derived from the downstream gene exons. [provided by RefSeq, Feb 2011]

ACMG classification

Our verdict: Likely_benign. The variant received -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001203260.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	NDUFC2-KCTD14	NM_001203260.2		c.311-13985A>T		intron	N/A	NP_001190189.1	A0A087WUM3
	NDUFC2-KCTD14	NM_001203261.2		c.310+20255A>T		intron	N/A	NP_001190190.1	E9PQ53-1
	NDUFC2-KCTD14	NM_001203262.2		c.167-13985A>T		intron	N/A	NP_001190191.1	A0A087WY27

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	NDUFC2-KCTD14	ENST00000530054.1	TSL:2	c.310+20255A>T		intron	N/A	ENSP00000432614.1	E9PQ53-1
	NDUFC2-KCTD14	ENST00000612612.5	TSL:2	c.311-13985A>T		intron	N/A	ENSP00000478766.1	A0A087WUM3
	NDUFC2-KCTD14	ENST00000614236.2	TSL:5	c.167-13985A>T		intron	N/A	ENSP00000481472.1	A0A087WY27

Frequencies

GnomAD3 genomes Cov.: 32

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

GnomAD4 genome Cov.: 32

Alfa AF: 0.00 Hom.: 1847

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	0.20
DANN	Benign	0.63
PhyloP100		-0.40

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

Other links and lift over

dbSNP: rs627297; hg19: chr11-77763789;