Variant #0001063977 (NC_000003.11:g.50369236G>A, NM_001206957.1:c.61C>T (RASSF1))

Chromosome 3
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.50369236G>A
DNA change (hg38) -
Published as RASSF1(NM_007182.5):c.514C>T (p.(Arg172Cys))
ISCN -
DB-ID RASSF1_000017
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) 0.0002 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RASSF1 NM_001206957.1 ?/. - c.61C>T r.(?) p.(Arg21Cys)
TUSC2 NM_007275.1 ?/. - c.-3706C>T r.(?) p.(=)


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