Variant #0000717120 (NC_000001.10:g.209788708G>A, NM_000228.2:c.3427C>T (LAMB3))

Chromosome 1
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.209788708G>A
DNA change (hg38) -
Published as LAMB3(NM_000228.3):c.3427C>T (p.R1143C)
ISCN -
DB-ID CAMK1G_000006
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) 6.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMB3 NM_000228.2 ?/. - c.3427C>T r.(?) p.(Arg1143Cys)
CAMK1G NM_020439.2 ?/. - c.*2361G>A r.(=) p.(=)


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