Variant #0000528218 (NC_000006.11:g.30885474G>A, NM_020442.4:c.876G>A (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.30885474G>A
DNA change (hg38) g.30917697G>A
Published as VARS2(NM_001167733.1):c.456G>A (p.(=))
ISCN -
DB-ID GTF2H4_000006
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) 0.00225 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-18 15:24:20 +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.*3714G>A r.(=) p.(=)
VARS2 NM_020442.4 -?/. - c.876G>A r.(?) p.(Val292=)


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