Variant #0000802473 (NC_000006.11:g.30883017A>G, NC_000006.11(NM_020442.4):c.283+3A>G (VARS2))

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.30883017A>G
DNA change (hg38) -
Published as VARS2(NM_001167734.1):c.373+3A>G, VARS2(NM_020442.4):c.283+3A>G (p.?)
ISCN -
DB-ID GTF2H4_000009 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) 0.00014 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 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GTF2H4 NM_001517.4 -?/. - c.*1257A>G r.(=) p.(=)
VARS2 NM_020442.4 -?/. - c.283+3A>G r.spl? p.?


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