Variant #0000617815 (NC_000019.9:g.50393216G>A, NM_024682.2:c.*1335G>A (TBC1D17))

Chromosome 19
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.50393216G>A
DNA change (hg38) g.49889959G>A
Published as IL4I1(NM_001258018.1):c.1481C>T (p.P494L)
ISCN -
DB-ID ATF5_000015
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 2019-12-04 15:24:38 +01:00 (CET)
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     
ATF5 NM_001193646.1 ?/. - c.-39561G>A r.(?) p.(=)
IL4I1 NM_001258017.1 ?/. - c.1481C>T r.(?) p.(Pro494Leu)
TBC1D17 NM_024682.2 ?/. - c.*1335G>A r.(=) p.(=)
NUP62 NM_153719.3 ?/. - c.*18280C>T r.(=) p.(=)


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