Variant #0000977152 (NC_000006.11:g.30879869C>T, NM_020442.4:c.-2280C>T (VARS2))

Chromosome 6
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.30879869C>T
DNA change (hg38) -
Published as GTF2H4(NM_001517.5):c.904C>T (p.(His302Tyr))
ISCN -
DB-ID GTF2H4_000010
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
GTF2H4 NM_001517.4 ?/. - c.904C>T r.(?) p.(His302Tyr)
VARS2 NM_020442.4 ?/. - c.-2280C>T r.(?) p.(=)


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