Variant #0000858760 (NC_000003.11:g.121712793G>A, NM_175924.3:c.671C>T (ILDR1))

Chromosome 3
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.121712793G>A
DNA change (hg38) -
Published as ILDR1(NM_001199799.1):c.803C>T (p.P268L)
ISCN -
DB-ID ILDR1_000041
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) 3.0E-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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ILDR1 NM_001199799.2 ?/. - c.803C>T r.(?) p.(Pro268Leu)
ILDR1 NM_175924.3 ?/. - c.671C>T r.(?) p.(Pro224Leu)


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