Variant #0000858936 (NC_000003.11:g.197677108G>C, NC_000003.11(NM_000996.2):c.-33+16G>C (RPL35A))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.197677108G>C
DNA change (hg38) -
Published as RPL35A(NM_000996.4):c.-33+16G>C
ISCN -
DB-ID IQCG_000011
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL35A NM_000996.2 -/. - c.-33+16G>C r.(=) p.(=)
IQCG NM_032263.3 -/. - c.-59-4551C>G r.(=) p.(=)


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