Variant #0000806196 (NC_000013.10:g.51484284C>T, NC_000013.10(NM_024570.3):c.64+8C>T (RNASEH2B))

Chromosome 13
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.51484284C>T
DNA change (hg38) -
Published as RNASEH2B(NM_001142279.2):c.64+8C>T, RNASEH2B(NM_024570.3):c.64+8C>T
ISCN -
DB-ID RNASEH2B_000069 See all 2 reported entries
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) 0.00023 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNASEH2B NM_024570.3 -?/. - c.64+8C>T r.(=) p.(=)
RNASEH2B-AS1 NR_046552.1 -?/. - n.230+335G>A r.(?) -


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