Variant #0000678524 (NC_000009.11:g.130263351G>A, NM_138361.5:c.1975G>A (LRSAM1))

Chromosome 9
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.130263351G>A
DNA change (hg38) -
Published as LRSAM1(NM_138361.5):c.1975G>A (p.V659M)
ISCN -
DB-ID FAM129B_000009
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) 0.00465 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM129B NM_022833.2 -/. - c.*5773C>T r.(=) p.(=)
LRSAM1 NM_138361.5 -/. - c.1975G>A r.(?) p.(Val659Met)


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