Variant #0000998287 (NC_000010.10:g.43606650C>T, NC_000010.10(NM_020975.4):c.1264-5C>T (RET))

Chromosome 10
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.43606650C>T
DNA change (hg38) -
Published as RET(NM_020630.4):c.1264-5C>T (p.?), RET(NM_020975.4):c.1264-5C>T, RET(NM_020975.6):c.1264-5C>T
ISCN -
DB-ID RET_000233 See all 4 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) 0.00821 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-08-28 13:16:32 +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     
RET NM_020975.4 -/. - c.1264-5C>T r.spl? p.?


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