Variant #0000530416 (NC_000007.13:g.107749668C>G, NM_007356.2:c.350G>C (LAMB4))

Chromosome 7
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.107749668C>G
DNA change (hg38) g.108109223C>G
Published as LAMB4(NM_007356.2):c.350G>C (p.(Arg117Thr)), LAMB4(NM_007356.3):c.350G>C (p.R117T)
ISCN -
DB-ID LAMB4_000014 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) 0.01416 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-06 12:43:26 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMB4 NM_007356.2 -?/. - c.350G>C r.(?) p.(Arg117Thr)


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