rs1202585

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_StrongBA1

The NM_032800.3(C1orf198):​c.333+712T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.255 in 152,064 control chromosomes in the GnomAD database, including 5,541 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 0.25 ( 5541 hom., cov: 32)

Consequence

C1orf198
NM_032800.3 intron

Scores

2

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: 0.629
Variant links:
Genes affected
C1orf198 (HGNC:25900): (chromosome 1 open reading frame 198) Located in cytosol. [provided by Alliance of Genome Resources, Apr 2022]

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -12 ACMG points.

BP4
Computational evidence support a benign effect (BayesDel_noAF=-0.82).
BA1
GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.312 is higher than 0.05.

Transcripts

RefSeq

Gene Transcript HGVSc HGVSp Effect #exon/exons MANE UniProt
C1orf198NM_032800.3 linkuse as main transcriptc.333+712T>G intron_variant ENST00000366663.10

Ensembl

Gene Transcript HGVSc HGVSp Effect #exon/exons TSL MANE Appris UniProt
C1orf198ENST00000366663.10 linkuse as main transcriptc.333+712T>G intron_variant 1 NM_032800.3 P1Q9H425-1
C1orf198ENST00000427697.2 linkuse as main transcriptc.-229+1344T>G intron_variant 2
C1orf198ENST00000470540.5 linkuse as main transcriptc.219+712T>G intron_variant 2 Q9H425-3
C1orf198ENST00000522201.1 linkuse as main transcriptc.204+712T>G intron_variant 3

Frequencies

GnomAD3 genomes
AF:
0.255
AC:
38691
AN:
151946
Hom.:
5541
Cov.:
32
show subpopulations
Gnomad AFR
AF:
0.161
Gnomad AMI
AF:
0.338
Gnomad AMR
AF:
0.290
Gnomad ASJ
AF:
0.358
Gnomad EAS
AF:
0.0282
Gnomad SAS
AF:
0.273
Gnomad FIN
AF:
0.224
Gnomad MID
AF:
0.415
Gnomad NFE
AF:
0.316
Gnomad OTH
AF:
0.302
We have no GnomAD4 exomes data on this position. Probably position not covered by the project.
GnomAD4 genome
AF:
0.255
AC:
38701
AN:
152064
Hom.:
5541
Cov.:
32
AF XY:
0.250
AC XY:
18587
AN XY:
74324
show subpopulations
Gnomad4 AFR
AF:
0.161
Gnomad4 AMR
AF:
0.290
Gnomad4 ASJ
AF:
0.358
Gnomad4 EAS
AF:
0.0280
Gnomad4 SAS
AF:
0.273
Gnomad4 FIN
AF:
0.224
Gnomad4 NFE
AF:
0.316
Gnomad4 OTH
AF:
0.301
Alfa
AF:
0.283
Hom.:
3159
Bravo
AF:
0.253
Asia WGS
AF:
0.178
AC:
617
AN:
3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name
Calibrated prediction
Score
Prediction
BayesDel_noAF
Benign
-0.82
CADD
Benign
6.4
DANN
Benign
0.59

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

Below is the list of publications found by LitVar. It may be empty.

Other links and lift over

dbSNP: rs1202585; hg19: chr1-231003214; API