Variant #0000297685 (NC_000011.9:g.65487567G>C, NM_032193.3:c.417C>G (RNASEH2C))

Chromosome 11
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.65487567G>C
DNA change (hg38) g.65720096G>C
Published as RNASEH2C(NM_032193.3):c.417C>G (p.G139=), RNASEH2C(NM_032193.4):c.417C>G (p.G139=)
ISCN -
DB-ID RNASEH2C_000023 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) 0.00249 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KAT5 NM_006388.3 -?/. - c.*915G>C r.(=) p.(=)
RNASEH2C NM_032193.3 -?/. - c.417C>G r.(?) p.(Gly139=)


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