Variant #0000324511 (NC_000016.9:g.2815872_2815873del, NM_016333.3:c.5343_5344del (SRRM2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2815872_2815873del
DNA change (hg38) g.2765871_2765872del
Published as SRRM2(NM_016333.3):c.5341_5342del (p.(Lys1781AsnfsTer9))
ISCN -
DB-ID SRRM2_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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +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.5343_5344del r.(?) p.(Lys1781AsnfsTer9)


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