Variant #0000526899 (NC_000006.11:g.112537641C>T, NM_001105206.2:c.225G>A (LAMA4))

Chromosome 6
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.112537641C>T
DNA change (hg38) g.112216440C>T
Published as LAMA4(NM_001105206.2):c.225G>A (p.L75=), LAMA4(NM_001105206.3):c.225G>A (p.L75=)
ISCN -
DB-ID LAMA4_000128 See all 3 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) 4.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-19 19:55:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMA4 NM_001105206.2 -/. - c.225G>A r.(?) p.(Leu75=)


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