Variant #0000617816 (NC_000019.9:g.50393407G>C, NM_024682.2:c.*1526G>C (TBC1D17))

Chromosome 19
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.50393407G>C
DNA change (hg38) g.49890150G>C
Published as IL4I1(NM_001258018.1):c.1290C>G (p.A430=)
ISCN -
DB-ID ATF5_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) 7.0E-5 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-16 11:01:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATF5 NM_001193646.1 -?/. - c.-39370G>C r.(?) p.(=)
IL4I1 NM_001258017.1 -?/. - c.1290C>G r.(?) p.(Ala430=)
TBC1D17 NM_024682.2 -?/. - c.*1526G>C r.(=) p.(=)
NUP62 NM_153719.3 -?/. - c.*18089C>G r.(=) p.(=)


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