Variant #0000308433 (NC_000017.10:g.7385778T>G, NM_000937.4:c.-2306T>G (POLR2A))

Chromosome 17
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.7385778T>G
DNA change (hg38) g.7482459T>G
Published as SLC35G6(NM_001102614.1):c.475T>G (p.W159G)
ISCN -
DB-ID SLC35G6_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) 0.00016 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 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     
POLR2A NM_000937.4 ?/. - c.-2306T>G r.(?) p.(=)
SLC35G6 NM_001102614.1 ?/. - c.475T>G r.(?) p.(Trp159Gly)
ZBTB4 NM_020899.3 ?/. - c.-81+1545A>C r.(=) p.(=)


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