Variant #0000608402 (NC_000003.11:g.167508341T>C, NM_001122752.1:c.432T>C (SERPINI1))

Chromosome 3
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.167508341T>C
DNA change (hg38) g.167790553T>C
Published as SERPINI1(NM_005025.4):c.432T>C (p.N144=), SERPINI1(NM_005025.5):c.432T>C (p.N144=)
ISCN -
DB-ID SERPINI1_000005 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) 0.00094 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 2019-12-04 14:54:23 +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.432T>C r.(?) p.(Asn144=)


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