Variant #0000608140 (NC_000002.11:g.86332852G>A, NM_015425.3:c.48C>T (POLR1A))

Chromosome 2
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.86332852G>A
DNA change (hg38) g.86105729G>A
Published as POLR1A(NM_015425.5):c.48C>T (p.S16=)
ISCN -
DB-ID POLR1A_000038
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) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLR1A NM_015425.3 -?/. - c.48C>T r.(?) p.(Ser16=)
PTCD3 NM_017952.5 -?/. - c.-519G>A r.(?) p.(=)


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