Variant #0000568090 (NC_000019.9:g.50435876T>C, NM_001193646.1:c.376T>C (ATF5))

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.50435876T>C
DNA change (hg38) g.49932619T>C
Published as ATF5(NM_001193646.1):c.376T>C (p.(Ser126Pro))
ISCN -
DB-ID ATF5_000012
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
ATF5 NM_001193646.1 -?/. - c.376T>C r.(?) p.(Ser126Pro)
IL4I1 NM_001258017.1 -?/. - c.-3619A>G r.(?) p.(=)
NUP62 NM_153719.3 -?/. - c.-3526A>G r.(?) p.(=)


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