Variant #0000514857 (NC_000002.11:g.220435000A>C, OBSL1(NM_001173408.1):c.955T>G)

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.220435000A>C
DNA change (hg38) g.219570278A>C
Published as OBSL1(NM_015311.2):c.955T>G (p.C319G)
ISCN -
DB-ID INHA_000010
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OBSL1 NM_001173408.1 -?/. - c.955T>G r.(?) p.(Cys319Gly)
INHA NM_002191.3 -?/. - c.-2097A>C r.(?) p.(=)