Variant #0000344952 (NC_000006.11:g.2955853G>A, NM_001195291.1:c.217C>T (SERPINB6))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2955853G>A
DNA change (hg38) g.2955619G>A
Published as -
ISCN -
DB-ID SERPINB6_000017
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) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERPINB6 NM_001195291.1 ?/. - c.217C>T r.(?) p.(Gln73Ter)
SERPINB6 NM_004568.5 ?/. - c.217C>T r.(?) p.(Gln73Ter)


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