Variant #0000553271 (NC_000014.8:g.89205343T>G, NM_024824.4:c.*127248T>G (ZC3H14))

Chromosome 14
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.89205343T>G
DNA change (hg38) g.88738999T>G
Published as EML5(NM_183387.3):c.727A>C (p.M243L)
ISCN -
DB-ID EML5_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) 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 2019-07-18 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     
ZC3H14 NM_024824.4 ?/. - c.*127248T>G r.(=) p.(=)
EML5 NM_183387.2 ?/. - c.727A>C r.(?) p.(Met243Leu)


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