Variant #0000299416 (NC_000011.9:g.75277757C>G, NM_001207014.1:c.363C>G (SERPINH1))

Chromosome 11
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.75277757C>G
DNA change (hg38) g.75566712C>G
Published as SERPINH1(NM_001207014.3):c.363C>G (p.S121=), SERPINH1(NM_001235.5):c.363C>G (p.S121=)
ISCN -
DB-ID SERPINH1_000003 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) 0.34597 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERPINH1 NM_001207014.1 -/. - c.363C>G r.(?) p.(Ser121=)


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