Variant #0000990263 (NC_000001.10:g.151143146G>A, NM_024041.3:c.*1585G>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.151143146G>A
DNA change (hg38) -
Published as TMOD4(NM_013353.2):c.871-7C>T (p.?)
ISCN -
DB-ID LYSMD1_000002
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     
TMOD4 NM_013353.2 ?/. - c.871-7C>T r.(=) p.(=)
SCNM1 NM_024041.3 ?/. - c.*1585G>A r.(=) p.(=)
TNFAIP8L2 NM_024575.4 ?/. - c.*11418G>A r.(=) p.(=)
LYSMD1 NM_212551.4 ?/. - c.-5412C>T r.(?) p.(=)


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