Variant #0000980857 (NC_000014.8:g.24001946C>T, NM_003917.2:c.*27012G>A (AP1G2))

Chromosome 14
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.24001946C>T
DNA change (hg38) -
Published as ZFHX2(NM_033400.3):c.2389G>A (p.(Gly797Arg))
ISCN -
DB-ID AP1G2_000014
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     
THTPA NM_001126339.2 ?/. - c.-23622C>T r.(?) p.(=)
AP1G2 NM_003917.2 ?/. - c.*27012G>A r.(=) p.(=)
ZFHX2 NM_033400.2 ?/. - c.2389G>A r.(?) p.(Gly797Arg)


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