Variant #0000894389 (NC_000018.9:g.12329644G>A, NM_006796.2:c.2314C>T (AFG3L2))

Chromosome 18
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.12329644G>A
DNA change (hg38) -
Published as AFG3L2(NM_006796.2):c.2314C>T (p.L772F), AFG3L2(NM_006796.3):c.2314C>T (p.L772F), TUBB6(NM_001303525.2):c.*462G>A
ISCN -
DB-ID AFG3L2_000022 See all 5 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) 0.00173 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AFG3L2 NM_006796.2 -?/. - c.2314C>T r.(?) p.(Leu772Phe)
TUBB6 NM_032525.1 -?/. - c.*3515G>A r.(=) p.(=)


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