Variant #0000505038 (NC_000001.10:g.209791358T>C, NM_000228.2:c.2945A>G (LAMB3))

Chromosome 1
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.209791358T>C
DNA change (hg38) g.209618013T>C
Published as LAMB3(NM_000228.3):c.2945A>G (p.D982G), LAMB3(NM_001017402.1):c.2945A>G (p.D982G)
ISCN -
DB-ID CAMK1G_000002 See all 2 reported entries
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) 0.00113 View details
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 2022-05-09 15:24:52 +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.2945A>G r.(?) p.(Asp982Gly)
CAMK1G NM_020439.2 -?/. - c.*5011T>C r.(=) p.(=)


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