Variant #0000502981 (NC_000001.10:g.145474625dup, NM_032305.1:c.-4342dup (POLR3GL))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.145474625dup
DNA change (hg38) -
Published as ANKRD34A(NM_001039888.2):c.1295dup (p.(His433ProfsTer6))
ISCN -
DB-ID POLR3GL_000005
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD34A NM_001039888.2 -?/. - c.1297dup r.(?) p.(His433ProfsTer6)
POLR3GL NM_032305.1 -?/. - c.-4342dup r.(?) p.(=)
LIX1L NM_153713.1 -?/. - c.-2534dup r.(?) p.(=)


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