Variant #0000554183 (NC_000015.9:g.41108163T>C, NM_001077268.1:c.*1739T>C (ZFYVE19))

Chromosome 15
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.41108163T>C
DNA change (hg38) g.40815965T>C
Published as PPP1R14D(NM_001130143.1):c.485A>G (p.(Gln162Arg))
ISCN -
DB-ID DNAJC17_000004
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) 0.00292 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-06 10:22:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZFYVE19 NM_001077268.1 -?/. - c.*1739T>C r.(=) p.(=)
PPP1R14D NM_017726.7 -?/. - c.369A>G r.(?) p.(Thr123=)
DNAJC17 NM_018163.2 -?/. - c.-8519A>G r.(?) p.(=)


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