Variant #0000692693 (NC_000019.9:g.12991950G>C, NM_001375.2:c.103C>G (DNASE2))

Chromosome 19
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.12991950G>C
DNA change (hg38) -
Published as DNASE2(NM_001375.3):c.103C>G (p.L35V)
ISCN -
DB-ID DNASE2_000007
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) 2.0E-5 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 2020-09-15 15:50:26 +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     
DNASE2 NM_001375.2 ?/. - c.103C>G r.(?) p.(Leu35Val)
KLF1 NM_006563.3 ?/. - c.*3749C>G r.(=) p.(=)


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