Variant #0000515145 (NC_000002.11:g.234217804_234217811del, NC_000002.11(NM_000541.4):c.-28-4_-25del (SAG))

Chromosome 2
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.234217804_234217811del
DNA change (hg38) g.233309158_233309165del
Published as SAG(NM_000541.4):c.-28-4_-25delCAAGGTGG
ISCN -
DB-ID SAG_000041
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-11 18:50:13 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SAG NM_000541.4 ?/. - c.-28-4_-25del r.spl? p.?


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