Variant #0000857528 (NC_000001.10:g.47133834C>T, NM_022745.4:c.230G>A (ATPAF1))

Chromosome 1
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.47133834C>T
DNA change (hg38) -
Published as ATPAF1(NM_022745.4):c.230G>A (p.G77D)
ISCN -
DB-ID ATPAF1_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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TEX38 NM_001145474.2 ?/. - c.-3773C>T r.(?) p.(=)
ATPAF1 NM_022745.4 ?/. - c.230G>A r.(?) p.(Gly77Asp)


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