Variant #0000554182 (NC_000015.9:g.41102314T>C, NM_001077268.1:c.617T>C (ZFYVE19))

Chromosome 15
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.41102314T>C
DNA change (hg38) g.40810116T>C
Published as ZFYVE19(NM_001077268.1):c.617T>C (p.(Leu206Pro))
ISCN -
DB-ID ZFYVE19_000001
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 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 2021-08-03 20:52:44 +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.617T>C r.(?) p.(Leu206Pro)
C15orf62 NM_001130448.2 ?/. - c.*39093T>C r.(=) p.(=)
DNAJC17 NM_018163.2 ?/. - c.-2670A>G r.(?) p.(=)


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