Variant #0000328457 (NC_000020.10:g.44574444G>A, NM_022095.3:c.*3148C>T (ZNF335))

Chromosome 20
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.44574444G>A
DNA change (hg38) g.45945805G>A
Published as PCIF1(NM_022104.3):c.1263G>A (p.(Met421Ile))
ISCN -
DB-ID PCIF1_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) 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 2018-01-15 20:58:59 +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     
ZNF335 NM_022095.3 ?/. - c.*3148C>T r.(=) p.(=)
PCIF1 NM_022104.3 ?/. - c.1263G>A r.(?) p.(Met421Ile)


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