Variant #0000565361 (NC_000018.9:g.7038788_7038790dup, NC_000018.9(NM_005559.3):c.1563+23_1563+25dup (LAMA1))

Chromosome 18
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.7038788_7038790dup
DNA change (hg38) g.7038789_7038791dup
Published as LAMA1(NM_005559.4):c.1563+22_1563+24dupGCG
ISCN -
DB-ID LAMA1_000163
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 2019-07-18 18:22:55 +02:00 (CEST)
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     
LAMA1 NM_005559.3 -/. - c.1563+23_1563+25dup r.(=) p.(=)


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