chr4-105713579-T-C

Variant names:

• chr4-105713579-T-C
• rs17036142
• NM_001370181.1:c.-21-4014T>C

Variant summary

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

The NM_001370181.1(GSTCD):​c.-21-4014T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0536 in 152,294 control chromosomes in the GnomAD database, including 253 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 0.054 (253 hom., cov: 32)
• Consequence: GSTCD NM_001370181.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.131
• Publications: 6 publications found

Genes affected

GSTCD (HGNC:25806): (glutathione S-transferase C-terminal domain containing) Located in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

INTS12 (HGNC:25067): (integrator complex subunit 12) INTS12 is a subunit of the Integrator complex, which associates with the C-terminal domain of RNA polymerase II large subunit (POLR2A; MIM 180660) and mediates 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) and U2 (RNU2; MIM 180690) (Baillat et al., 2005 [PubMed 16239144]).[supplied by OMIM, Mar 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.0659 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001370181.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GSTCD	NM_001370181.1	MANE Select	c.-21-4014T>C		intron	N/A	NP_001357110.1
	GSTCD	NM_001031720.3		c.-22+2716T>C		intron	N/A	NP_001026890.2
	GSTCD	NM_024751.3		c.-21-4014T>C		intron	N/A	NP_079027.2

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GSTCD	ENST00000515279.6	TSL:5 MANE Select	c.-21-4014T>C		intron	N/A	ENSP00000422354.1
	GSTCD	ENST00000360505.9	TSL:1	c.-22+2716T>C		intron	N/A	ENSP00000353695.5
	GSTCD	ENST00000394728.4	TSL:5	c.-22+977T>C		intron	N/A	ENSP00000378216.3

Frequencies

GnomAD3 genomes AF: 0.0537 AC: 8166 AN: 152176 Hom.: 254 Cov.: 32

Gnomad AFR AF: 0.0408

Gnomad AMI AF: 0.136

Gnomad AMR AF: 0.0696

Gnomad ASJ AF: 0.0815

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.0209

Gnomad FIN AF: 0.0317

Gnomad MID AF: 0.149

Gnomad NFE AF: 0.0641

Gnomad OTH AF: 0.0760

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

GnomAD4 genome AF: 0.0536 AC: 8164 AN: 152294 Hom.: 253 Cov.: 32 AF XY: 0.0511 AC XY: 3808 AN XY: 74476

African (AFR) AF: 0.0408 AC: 1696 AN: 41570

American (AMR) AF: 0.0694 AC: 1062 AN: 15300

Ashkenazi Jewish (ASJ) AF: 0.0815 AC: 283 AN: 3472

East Asian (EAS) AF: 0.00 AC: 0 AN: 5192

South Asian (SAS) AF: 0.0209 AC: 101 AN: 4826

European-Finnish (FIN) AF: 0.0317 AC: 336 AN: 10614

Middle Eastern (MID) AF: 0.136 AC: 40 AN: 294

European-Non Finnish (NFE) AF: 0.0641 AC: 4362 AN: 68000

Other (OTH) AF: 0.0757 AC: 160 AN: 2114

Alfa AF: 0.0563 Hom.: 60

Bravo AF: 0.0563

Asia WGS AF: 0.0140 AC: 48 AN: 3466

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	3.2
DANN	Benign	0.73
PhyloP100		0.13
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: rs17036142; hg19: chr4-106634736;