chr11-18349351-G-C

Variant names:

• chr11-18349351-G-C
• rs4150642
• NM_005316.4:c.1053+1432G>C

Variant summary

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

The NM_005316.4(GTF2H1):​c.1053+1432G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.865 in 152,274 control chromosomes in the GnomAD database, including 57,348 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 0.87 (57348 hom., cov: 32)
• Consequence: GTF2H1 NM_005316.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0660
• Publications: 16 publications found

Genes affected

GTF2H1 (HGNC:4655): (general transcription factor IIH subunit 1) Enables thyroid hormone receptor binding activity. Involved in positive regulation of transcription, DNA-templated and transcription by RNA polymerase II. Located in nucleoplasm. Part of transcription factor TFIIH core complex and transcription factor TFIIH holo complex. [provided by Alliance of Genome Resources, Apr 2022]

LOC105376577 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.03).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.946 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_005316.4. 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
	GTF2H1	NM_005316.4	MANE Select	c.1053+1432G>C		intron	N/A	NP_005307.1
	GTF2H1	NM_001142307.2		c.1053+1432G>C		intron	N/A	NP_001135779.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GTF2H1	ENST00000265963.9	TSL:1 MANE Select	c.1053+1432G>C		intron	N/A	ENSP00000265963.4
	GTF2H1	ENST00000928992.1		c.1086+1432G>C		intron	N/A	ENSP00000599051.1
	GTF2H1	ENST00000453096.6	TSL:2	c.1053+1432G>C		intron	N/A	ENSP00000393638.2

Frequencies

GnomAD3 genomes AF: 0.865 AC: 131637 AN: 152156 Hom.: 57293 Cov.: 32

Gnomad AFR AF: 0.950

Gnomad AMI AF: 0.820

Gnomad AMR AF: 0.835

Gnomad ASJ AF: 0.726

Gnomad EAS AF: 0.968

Gnomad SAS AF: 0.794

Gnomad FIN AF: 0.868

Gnomad MID AF: 0.703

Gnomad NFE AF: 0.827

Gnomad OTH AF: 0.830

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

GnomAD4 genome AF: 0.865 AC: 131753 AN: 152274 Hom.: 57348 Cov.: 32 AF XY: 0.865 AC XY: 64380 AN XY: 74456

African (AFR) AF: 0.950 AC: 39496 AN: 41572

American (AMR) AF: 0.834 AC: 12764 AN: 15296

Ashkenazi Jewish (ASJ) AF: 0.726 AC: 2518 AN: 3470

East Asian (EAS) AF: 0.968 AC: 5021 AN: 5186

South Asian (SAS) AF: 0.794 AC: 3826 AN: 4816

European-Finnish (FIN) AF: 0.868 AC: 9209 AN: 10608

Middle Eastern (MID) AF: 0.694 AC: 204 AN: 294

European-Non Finnish (NFE) AF: 0.827 AC: 56210 AN: 68008

Other (OTH) AF: 0.832 AC: 1759 AN: 2114

Alfa AF: 0.803 Hom.: 2458

Bravo AF: 0.868

Asia WGS AF: 0.917 AC: 3186 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	2.0
DANN	Benign	0.35
PhyloP100		0.066
Mutation Taster		=100/0	polymorphism (auto)

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: rs4150642; hg19: chr11-18370898;