Variant #0000960491 (NC_000001.10:g.151134589dup, NM_024041.3:c.-4040dup (SCNM1))

Chromosome 1
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.151134589dup
DNA change (hg38) -
Published as LYSMD1(NM_212551.5):c.181-4dupT
ISCN -
DB-ID LYSMD1_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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +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     
TMOD4 NM_013353.2 -?/. - c.*7977dup r.(?) p.(=)
SCNM1 NM_024041.3 -?/. - c.-4040dup r.(?) p.(=)
TNFAIP8L2 NM_024575.4 -?/. - c.*2861dup r.(?) p.(=)
LYSMD1 NM_212551.4 -?/. - c.181-4dup r.spl? p.?


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