Variant #0000716800 (NC_000001.10:g.151143398G>A, NM_024041.3:c.*1837G>A (SCNM1))

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.151143398G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID TMOD4_000001
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2022-09-13 21:05:04 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMOD4 NM_013353.2 ?/. - c.868C>T r.(?) p.(Gln290*)
SCNM1 NM_024041.3 ?/. - c.*1837G>A r.(=) p.(=)
TNFAIP8L2 NM_024575.4 ?/. - c.*11670G>A r.(=) p.(=)
LYSMD1 NM_212551.4 ?/. - c.-5664C>T r.(?) p.(=)


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