Variant #0000928655 (NC_000002.11:g.73675776A>G, NM_001378454.1:c.2122A>G (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.73675776A>G
DNA change (hg38) g.73448649A>G
Published as ALMS1(NM_015120.4):c.2125A>G (p.(Thr709Ala))
ISCN -
DB-ID ALMS1_000843
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) 0.00029 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-07-07 10:10:56 +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.2122A>G r.(?) p.(Thr708Ala)


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