Variant #0000677725 (NC_000006.11:g.31910762_31910765del, NM_000063.4:c.1246_1249del (C2))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.31910762_31910765del
DNA change (hg38) -
Published as C2(NM_001282458.1):c.1159_1162delCTGG (p.L387Mfs*7)
ISCN -
DB-ID C2_000036
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C2 NM_000063.4 +/. - c.1246_1249del r.(?) p.(Leu416MetfsTer7)
CFB NM_001710.5 +/. - c.-3237_-3234del r.(?) p.(=)
ZBTB12 NM_181842.2 +/. - c.-41171_-41168del r.(?) p.(=)


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