Variant #0000248968 (NC_000001.10:g.209792016dup, NC_000001.10(NM_000228.2):c.2702-12dup (LAMB3))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.209792016dup
DNA change (hg38) g.209618671dup
Published as LAMB3(NM_001017402.2):c.2702-12dupG, LAMB3(NM_001017402.2):c.2702-13delTinsTG
ISCN -
DB-ID CAMK1G_000005
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMB3 NM_000228.2 -/. - c.2702-12dup r.(=) p.(=)
CAMK1G NM_020439.2 -/. - c.*5669dup r.(?) p.(=)


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