Variant #0000605732 (NC_000001.10:g.38018312_38018314del, NM_024700.3:c.264_266del (SNIP1))

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.38018312_38018314del
DNA change (hg38) g.37552711_37552713del
Published as SNIP1(NM_024700.3):c.264_266del (p.(Arg88del))
ISCN -
DB-ID DNALI1_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNALI1 NM_003462.3 ?/. - c.-4218_-4216del r.(?) p.(=)
GNL2 NM_013285.2 ?/. - c.*14147_*14149del r.(=) p.(=)
SNIP1 NM_024700.3 ?/. - c.264_266del r.(?) p.(Arg88del)


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