Variant #0001000942 (NC_000014.8:g.24029598G>A, NM_003917.2:c.2023C>T (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.24029598G>A
DNA change (hg38) -
Published as AP1G2(NM_003917.2):c.2023C>T (p.(Arg675Cys))
ISCN -
DB-ID AP1G2_000016
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 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 2024-08-28 13:16:32 +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.*1549G>A r.(=) p.(=)
AP1G2 NM_003917.2 ?/. - c.2023C>T r.(?) p.(Arg675Cys)
JPH4 NM_032452.2 ?/. - c.*9245C>T r.(=) p.(=)
ZFHX2 NM_033400.2 ?/. - c.-9096C>T r.(?) p.(=)


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