Variant #0000326077 (NC_000019.9:g.5679648C>T, NM_205767.1:c.156G>A (C19orf70))

Chromosome 19
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.5679648C>T
DNA change (hg38) g.5679637C>T
Published as C19orf70(NM_205767.1):c.156G>A (p.(Met52Ile))
ISCN -
DB-ID C19orf70_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) 2.0E-5 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     
HSD11B1L NM_198706.2 ?/. - c.-1649C>T r.(?) p.(=)
C19orf70 NM_205767.1 ?/. - c.156G>A r.(?) p.(Met52Ile)


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