Variant #0000335965 (NC_000023.10:g.152110301A>G, NC_000023.10(NM_001178106.1):c.1305-3510A>G (ZNF185))

Chromosome X
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.152110301A>G
DNA change (hg38) g.152941757A>G
Published as ZNF185(NM_001178115.1):c.49A>G (p.(Met17Val))
ISCN -
DB-ID ZNF185_000057
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) 0.00377 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 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     
ZNF185 NM_001178106.1 ?/. - c.1305-3510A>G r.(=) p.(=)


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