Variant #0000617535 (NC_000019.9:g.35739926A>T, NM_205834.3:c.145A>T (LSR))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.35739926A>T
DNA change (hg38) g.35249023A>T
Published as LSR(NM_205834.3):c.145A>T (p.M49L)
ISCN -
DB-ID LSR_000006
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LSR NM_015925.5 ?/. - c.145A>T r.(?) p.(Met49Leu)
LSR NM_205834.3 ?/. - c.145A>T r.(?) p.(Met49Leu)


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