Variant #0000802464 (NC_000006.11:g.2948568G>A, NM_001195291.1:c.1095C>T (SERPINB6))

Chromosome 6
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.2948568G>A
DNA change (hg38) -
Published as SERPINB6(NM_001297699.1):c.1095C>T (p.N365=)
ISCN -
DB-ID SERPINB6_000020 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) 0.00143 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERPINB6 NM_001195291.1 -?/. - c.1095C>T r.(?) p.(Asn365=)
SERPINB6 NM_004568.5 -?/. - c.1095C>T r.(?) p.(Asn365=)


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