Variant #0000557723 (NC_000016.9:g.2813386_2813387del, NM_016333.3:c.2857_2858del (SRRM2))

Chromosome 16
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.2813386_2813387del
DNA change (hg38) g.2763385_2763386del
Published as SRRM2(NM_016333.4):c.2857_2858delGT (p.V953Ifs*29)
ISCN -
DB-ID SRRM2_000014
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_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 2020-07-09 11:09:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SRRM2 NM_016333.3 ?/. - c.2857_2858del r.(?) p.(Val953IlefsTer29)


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