Variant #0000327391 (NC_000002.11:g.152584331_152584345del, NM_001271208.1:c.169_183del (NEB))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.152584331_152584345del
DNA change (hg38) g.151727817_151727831del
Published as NEB(NM_001164507.1):c.169_183del (p.(Leu57_Ala61del)), NEB(NM_001271208.1):c.169_183delCTGGCACAGCCAGCA (p.L57_A61del)
ISCN -
DB-ID NEB_000496
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 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
NEB NM_001271208.1 -?/. - c.169_183del - r.(?) p.(Leu57_Ala61del)


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