Variant #0000346746 (NC_000007.13:g.127669210_127669213del, NM_022143.4:c.1484_1487del (LRRC4))

Chromosome 7
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.127669210_127669213del
DNA change (hg38) g.128029157_128029160del
Published as -
ISCN -
DB-ID SND1_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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-23 14:04:16 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SND1 NM_014390.2 ?/. - c.1779+38101_1779+38104del r.(=) p.(=)
LRRC4 NM_022143.4 ?/. - c.1484_1487del r.(?) p.(Ile495ArgfsTer28)


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