rs708384

Variant names:

• chr17-44360314-C-A
• rs708384
• NM_198475.3:c.119-182G>T

Your query was ambiguous. Multiple possible variants found:

• chr17-44360314-C-A
• chr17-44360314-C-T

Variant summary

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

The NM_198475.3(FAM171A2):​c.119-182G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.462 in 152,142 control chromosomes in the GnomAD database, including 18,232 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 0.46 (18232 hom., cov: 33)
• Consequence: FAM171A2 NM_198475.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.104
• Publications: 17 publications found

Genes affected

FAM171A2 (HGNC:30480): (family with sequence similarity 171 member A2) Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.711 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_198475.3. 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
	FAM171A2	NM_198475.3	MANE Select	c.119-182G>T		intron	N/A	NP_940877.2

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FAM171A2	ENST00000293443.12	TSL:1 MANE Select	c.119-182G>T		intron	N/A	ENSP00000293443.6
	FAM171A2	ENST00000588067.1	TSL:5	n.119-182G>T		intron	N/A	ENSP00000466493.1
	FAM171A2	ENST00000589407.5	TSL:3	n.119-182G>T		intron	N/A	ENSP00000466195.1

Frequencies

GnomAD3 genomes AF: 0.462 AC: 70182 AN: 152024 Hom.: 18209 Cov.: 33

Gnomad AFR AF: 0.718

Gnomad AMI AF: 0.413

Gnomad AMR AF: 0.303

Gnomad ASJ AF: 0.415

Gnomad EAS AF: 0.376

Gnomad SAS AF: 0.326

Gnomad FIN AF: 0.417

Gnomad MID AF: 0.329

Gnomad NFE AF: 0.370

Gnomad OTH AF: 0.406

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

GnomAD4 genome AF: 0.462 AC: 70245 AN: 152142 Hom.: 18232 Cov.: 33 AF XY: 0.456 AC XY: 33921 AN XY: 74370

African (AFR) AF: 0.718 AC: 29801 AN: 41510

American (AMR) AF: 0.303 AC: 4621 AN: 15276

Ashkenazi Jewish (ASJ) AF: 0.415 AC: 1441 AN: 3470

East Asian (EAS) AF: 0.375 AC: 1945 AN: 5180

South Asian (SAS) AF: 0.324 AC: 1563 AN: 4822

European-Finnish (FIN) AF: 0.417 AC: 4414 AN: 10580

Middle Eastern (MID) AF: 0.327 AC: 96 AN: 294

European-Non Finnish (NFE) AF: 0.370 AC: 25139 AN: 67988

Other (OTH) AF: 0.402 AC: 848 AN: 2110

Alfa AF: 0.371 Hom.: 19480

Bravo AF: 0.463

Asia WGS AF: 0.382 AC: 1336 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	0.48
DANN	Benign	0.45
PhyloP100		-0.10
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: rs708384; hg19: chr17-42437682;