Variant #0000990256 (NC_000001.10:g.149897723C>A, NC_000001.10(NM_005850.4):c.913+5G>T (SF3B4))

Chromosome 1
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.149897723C>A
DNA change (hg38) -
Published as SF3B4(NM_005850.4):c.913+5G>T (p.?)
ISCN -
DB-ID MTMR11_000016
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) 1.0E-5 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 2024-08-28 13:07:21 +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     
MTMR11 NM_001145862.1 ?/. - c.*3298G>T r.(=) p.(=)
SF3B4 NM_005850.4 ?/. - c.913+5G>T r.spl? p.?
MTMR11 NM_181873.3 ?/. - c.*3036G>T r.(=) p.(=)


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