Variant #0001014582 (NC_000010.10:g.104263959C>T, NM_016169.3:c.50C>T (SUFU))

Chromosome 10
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.104263959C>T
DNA change (hg38) -
Published as SUFU(NM_016169.3):c.50C>T (p.A17V), SUFU(NM_016169.4):c.50C>T (p.A17V)
ISCN -
DB-ID ACTR1A_000008 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) 0.00022 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 2024-10-29 21:08:56 +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     
ACTR1A NM_005736.3 ?/. - c.-1555G>A r.(?) p.(=)
SUFU NM_016169.3 ?/. - c.50C>T r.(?) p.(Ala17Val)


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