Variant #0000884931 (NC_000002.11:g.220418334C>A, NM_015311.2:c.4951G>T (OBSL1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.220418334C>A
DNA change (hg38) -
Published as OBSL1(NM_015311.2):c.4951G>T (p.(Glu1651*))
ISCN -
DB-ID CHPF_000021 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00162 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM198 NM_001005209.1 -?/. - c.*3758C>A r.(=) p.(=)
OBSL1 NM_015311.2 -?/. - c.4951G>T r.(?) p.(Glu1651*)
CHPF NM_024536.5 -?/. - c.-10074G>T r.(?) p.(=)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.