Variant #0000323609 (NC_000014.8:g.24002560C>T, NM_003917.2:c.*26398G>A (AP1G2))

Chromosome 14
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.24002560C>T
DNA change (hg38) g.23533351C>T
Published as ZFHX2(NM_033400.3):c.1975G>A (p.(Glu659Lys))
ISCN -
DB-ID AP1G2_000004
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) 0.00041 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
THTPA NM_001126339.2 -?/. - c.-23008C>T r.(?) p.(=)
AP1G2 NM_003917.2 -?/. - c.*26398G>A r.(=) p.(=)
ZFHX2 NM_033400.2 -?/. - c.1975G>A r.(?) p.(Glu659Lys)


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