Variant #0000564216 (NC_000018.9:g.21511172G>T, LAMA3(NM_198129.1):c.8576+7G>T)

Chromosome 18
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.21511172G>T
DNA change (hg38) g.23931208G>T
Published as LAMA3(NM_000227.3):c.3749+7G>T (p.(=)), LAMA3(NM_198129.2):c.8576+7G>T
ISCN -
DB-ID LAMA3_000039 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) 0.00245 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 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     
LAMA3 NM_198129.1 -?/. - c.8576+7G>T r.(=) p.(=)