Variant #0000525305 (NC_000005.9:g.176729749T>C, NM_022455.4:c.*7289T>C (NSD1))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.176729749T>C
DNA change (hg38) g.177302748T>C
Published as RAB24(NM_001031677.2):c.265+4A>G (p.?)
ISCN -
DB-ID NSD1_000231
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MXD3 NM_001142935.1 -?/. - c.*4371A>G r.(=) p.(=)
PRELID1 NM_013237.2 -?/. - c.-1238T>C r.(?) p.(=)
NSD1 NM_022455.4 -?/. - c.*7289T>C r.(=) p.(=)
RAB24 NM_130781.2 -?/. - c.265+4A>G r.spl? p.?


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