NM_006323.5:c.16G>C

Variant names:

• chr4-109433885-G-C
• rs2125881864
• NM_006323.5:c.16G>C

Variant summary

Our verdict is Uncertain significance. The variant received 1 ACMG points: 2P and 1B. PM2 BP4

The NM_006323.5(SEC24B):​c.16G>C​(p.Gly6Arg) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000000839 in 1,191,758 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).

• Frequency:
  • Genomes: not found (cov: 31)
  • Exomes 𝑓: 8.4e-7 (0 hom.)
• Consequence: SEC24B NM_006323.5 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 3.45
• Publications: 0 publications found

Genes affected

SEC24B (HGNC:10704): (SEC24 homolog B, COPII coat complex component) The protein encoded by this gene is a member of the SEC24 subfamily of the SEC23/SEC24 family, which is involved in vesicle trafficking. The encoded protein is thought to be a cargo-binding component of the COPII vesicle, and is thought to be involved in the transport of secretory proteins from the endoplasmic reticulum to the Golgi apparatus. Mutations in this gene have been associated with neural tube defects, and are thought to be a result of a disruption in interactions with the protein encoded by the VANGL planar cell polarity protein 2 (VANGL2) gene. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]

SEC24B-AS1 (HGNC:44003): (SEC24B antisense RNA 1) This lncRNA contains a single Alu element which, along with 1/2-sbsRNA3, appears to target the 3' UTR Alu element in MTAP. Downregulation of the RNA appears to up-regulate the target. [provided by RefSeq, Feb 2011]

ACMG classification

Our verdict: Uncertain_significance. The variant received 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.28327566).

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_006323.5. 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
	SEC24B	NM_006323.5	MANE Select	c.16G>C	p.Gly6Arg	missense	Exon 1 of 24	NP_006314.2	O95487-1
	SEC24B	NM_001300813.3		c.16G>C	p.Gly6Arg	missense	Exon 1 of 25	NP_001287742.1	O95487-3
	SEC24B	NM_001318085.2		c.16G>C	p.Gly6Arg	missense	Exon 1 of 24	NP_001305014.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SEC24B	ENST00000265175.5	TSL:1 MANE Select	c.16G>C	p.Gly6Arg	missense	Exon 1 of 24	ENSP00000265175.4	O95487-1
	SEC24B	ENST00000504968.6	TSL:1	c.16G>C	p.Gly6Arg	missense	Exon 1 of 25	ENSP00000428564.1	O95487-3
	SEC24B	ENST00000399100.6	TSL:1	c.16G>C	p.Gly6Arg	missense	Exon 1 of 23	ENSP00000382051.2	O95487-2

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome AF: 8.39e-7 AC: 1 AN: 1191758 Hom.: 0 Cov.: 30 AF XY: 0.00 AC XY: 0 AN XY: 582976

African (AFR) AF: 0.00 AC: 0 AN: 24228

American (AMR) AF: 0.00 AC: 0 AN: 17510

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 19050

East Asian (EAS) AF: 0.0000383 AC: 1 AN: 26112

South Asian (SAS) AF: 0.00 AC: 0 AN: 51796

European-Finnish (FIN) AF: 0.00 AC: 0 AN: 26826

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 3302

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 975648

Other (OTH) AF: 0.00 AC: 0 AN: 47286

GnomAD4 genome Cov.: 31

ClinVar

ClinVar submissions

Significance: Uncertain significance

Revision: criteria provided, single submitter

Pathogenic	VUS	Benign	Condition
-	1	-	not specified (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Uncertain	0.37
BayesDel_addAF	Pathogenic	0.17	D
BayesDel_noAF	Uncertain	0.010
CADD	Uncertain	24
DANN	Uncertain	1.0
DEOGEN2	Benign	0.11	T
Eigen	Benign	-0.13
Eigen_PC	Benign	-0.070
FATHMM_MKL	Benign	0.27	N
LIST_S2	Benign	0.55	T
M_CAP	Pathogenic	0.97	D
MetaRNN	Benign	0.28	T
MetaSVM	Uncertain	0.075	D
MutationAssessor	Benign	0.90	L
PhyloP100		3.4
PrimateAI	Pathogenic	0.87	D
PROVEAN	Benign	-0.58	N
REVEL	Benign	0.28
Sift	Uncertain	0.0030	D
Sift4G	Benign	0.063	T
Polyphen		0.70	P
Vest4		0.24
MutPred		0.27		Gain of MoRF binding (P = 2e-04)
MVP		0.51
MPC		0.17
ClinPred		0.81	D
GERP RS		3.1
PromoterAI		-0.072	Neutral
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.7
Varity_R		0.16
gMVP		0.24
Mutation Taster		=91/9	polymorphism

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: rs2125881864; hg19: chr4-110355041;