rs1563824

Variant names:

• chr10-59272506-G-A
• rs1563824
• NM_198215.4:c.593-2397C>T

Your query was ambiguous. Multiple possible variants found:

• chr10-59272506-G-A
• chr10-59272506-G-T

Variant summary

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

The NM_198215.4(FAM13C):​c.593-2397C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.232 in 152,112 control chromosomes in the GnomAD database, including 5,495 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 0.23 (5495 hom., cov: 32)
• Consequence: FAM13C NM_198215.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.300
• Publications: 0 publications found

Genes affected

FAM13C (HGNC:19371): (family with sequence similarity 13 member C)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.433 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_198215.4. 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
	FAM13C	NM_198215.4	MANE Select	c.593-2397C>T		intron	N/A	NP_937858.2	Q8NE31-1
	FAM13C	NM_001347852.2		c.593-2397C>T		intron	N/A	NP_001334781.1	B7Z2K3
	FAM13C	NM_001347849.2		c.593-2397C>T		intron	N/A	NP_001334778.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FAM13C	ENST00000618804.5	TSL:1 MANE Select	c.593-2397C>T		intron	N/A	ENSP00000481854.1	Q8NE31-1
	FAM13C	ENST00000611933.4	TSL:1	c.593-2397C>T		intron	N/A	ENSP00000481830.1	Q8NE31-3
	FAM13C	ENST00000951024.1		c.593-2397C>T		intron	N/A	ENSP00000621083.1

Frequencies

GnomAD3 genomes AF: 0.231 AC: 35142 AN: 151994 Hom.: 5471 Cov.: 32

Gnomad AFR AF: 0.438

Gnomad AMI AF: 0.121

Gnomad AMR AF: 0.147

Gnomad ASJ AF: 0.188

Gnomad EAS AF: 0.104

Gnomad SAS AF: 0.279

Gnomad FIN AF: 0.112

Gnomad MID AF: 0.172

Gnomad NFE AF: 0.154

Gnomad OTH AF: 0.197

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

GnomAD4 genome AF: 0.232 AC: 35216 AN: 152112 Hom.: 5495 Cov.: 32 AF XY: 0.228 AC XY: 16955 AN XY: 74356

African (AFR) AF: 0.439 AC: 18193 AN: 41480

American (AMR) AF: 0.147 AC: 2245 AN: 15274

Ashkenazi Jewish (ASJ) AF: 0.188 AC: 653 AN: 3470

East Asian (EAS) AF: 0.104 AC: 537 AN: 5170

South Asian (SAS) AF: 0.280 AC: 1348 AN: 4818

European-Finnish (FIN) AF: 0.112 AC: 1183 AN: 10594

Middle Eastern (MID) AF: 0.171 AC: 50 AN: 292

European-Non Finnish (NFE) AF: 0.154 AC: 10478 AN: 67988

Other (OTH) AF: 0.198 AC: 419 AN: 2114

Alfa AF: 0.200 Hom.: 508

Bravo AF: 0.242

Asia WGS AF: 0.224 AC: 781 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	0.66
DANN	Benign	0.21
PhyloP100		-0.30
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: rs1563824; hg19: chr10-61032266; COSMIC: COSV53249300; COSMIC: COSV53249300;