14-94322004-C-T

Position:

• chr14-94322004-C-T

Variant summary

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

The NM_001756.4(SERPINA6):​c.-20+1263G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.2 in 152,146 control chromosomes in the GnomAD database, including 3,437 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 0.20 (3437 hom., cov: 33)
• Consequence: SERPINA6 NM_001756.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.665

Genes affected

SERPINA6 (HGNC:1540): (serpin family A member 6) This gene encodes an alpha-globulin protein with corticosteroid-binding properties. This is the major transport protein for glucorticoids and progestins in the blood of most vertebrates. The gene localizes to a chromosomal region containing several closely related serine protease inhibitors which may have evolved by duplication events. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.38 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
SERPINA6	NM_001756.4	c.-20+1263G>A		intron_variant		ENST00000341584.4	NP_001747.3
SERPINA6	XM_047431827.1	c.-20+1263G>A		intron_variant			XP_047287783.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
SERPINA6	ENST00000341584.4	c.-20+1263G>A		intron_variant		1	NM_001756.4	ENSP00000342850	P1
SERPINA6	ENST00000557225.1	c.-188+1263G>A		intron_variant		2		ENSP00000452018
SERPINA6	ENST00000555056.1	c.-20+1263G>A		intron_variant, NMD_transcript_variant		2		ENSP00000451045

Frequencies

GnomAD3 genomes AF: 0.200 AC: 30461 AN: 152028 Hom.: 3428 Cov.: 33

Gnomad AFR AF: 0.150

Gnomad AMI AF: 0.303

Gnomad AMR AF: 0.150

Gnomad ASJ AF: 0.204

Gnomad EAS AF: 0.395

Gnomad SAS AF: 0.357

Gnomad FIN AF: 0.212

Gnomad MID AF: 0.239

Gnomad NFE AF: 0.213

Gnomad OTH AF: 0.206

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

GnomAD4 genome AF: 0.200 AC: 30489 AN: 152146 Hom.: 3437 Cov.: 33 AF XY: 0.203 AC XY: 15092 AN XY: 74364

Gnomad4 AFR AF: 0.150

Gnomad4 AMR AF: 0.149

Gnomad4 ASJ AF: 0.204

Gnomad4 EAS AF: 0.395

Gnomad4 SAS AF: 0.357

Gnomad4 FIN AF: 0.212

Gnomad4 NFE AF: 0.213

Gnomad4 OTH AF: 0.215

Alfa AF: 0.129 Hom.: 278

Bravo AF: 0.189

Asia WGS AF: 0.351 AC: 1220 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	2.8
DANN	Benign	0.53

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: rs941599; hg19: chr14-94788341;