Variant #0000299422 (NC_000003.11:g.167506937C>G, NM_001122752.1:c.21C>G (SERPINI1))

Chromosome 3
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.167506937C>G
DNA change (hg38) g.167789149C>G
Published as SERPINI1(NM_005025.4):c.21C>G (p.F7L), SERPINI1(NM_005025.5):c.21C>G (p.F7L)
ISCN -
DB-ID SERPINI1_000001 See all 2 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) 0.09943 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     
SERPINI1 NM_001122752.1 -/. - c.21C>G r.(?) p.(Phe7Leu)


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