Variant #0000552412 (NC_000014.8:g.23995073G>C, NM_003917.2:c.*33885C>G (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.23995073G>C
DNA change (hg38) g.23525864G>C
Published as ZFHX2(NM_033400.3):c.4078C>G (p.Q1360E)
ISCN -
DB-ID AP1G2_000002
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) 0.00032 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
THTPA NM_001126339.2 -?/. - c.-30495G>C r.(?) p.(=)
AP1G2 NM_003917.2 -?/. - c.*33885C>G r.(=) p.(=)
ZFHX2 NM_033400.2 -?/. - c.4078C>G r.(?) p.(Gln1360Glu)


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