Variant #0000858680 (NC_000002.11:g.73676909G>T, NM_001378454.1:c.3255G>T (ALMS1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.73676909G>T
DNA change (hg38) g.73449782G>T
Published as ALMS1(NM_015120.4):c.3258G>T (p.Q1086H)
ISCN -
DB-ID ALMS1_000801
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) 6.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2024-05-17 21:20:31 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALMS1 NM_001378454.1 -?/. - c.3255G>T r.(?) p.(Gln1085His)


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