Variant #0000910954 (NC_000001.10:g.228399482C>G, NM_001271223.2:c.-3C>G (OBSCN))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.228399482C>G
DNA change (hg38) -
Published as OBSCN(NM_052843.4):c.-3C>G
ISCN -
DB-ID C1orf145_000001
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) 0.64801 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OBSCN NM_001271223.2 -/. - c.-3C>G r.(?) p.(=)
C1orf145 NR_073155.1 -/. - n.234+1641G>C r.(?) -


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