Variant #0000611861 (NC_000009.11:g.130265060T>G, NM_138361.5:c.2054T>G (LRSAM1))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.130265060T>G
DNA change (hg38) g.127502781T>G
Published as LRSAM1(NM_138361.5):c.2054T>G (p.M685R)
ISCN -
DB-ID LRSAM1_000008 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM129B NM_022833.2 +/. - c.*4064A>C r.(=) p.(=)
LRSAM1 NM_138361.5 +/. - c.2054T>G r.(?) p.(Met685Arg)


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