Variant #0000982958 (NC_000018.9:g.12329618_12329629del, NM_006796.2:c.2334_2345del (AFG3L2))

Chromosome 18
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.12329618_12329629del
DNA change (hg38) -
Published as AFG3L2(NM_006796.3):c.2334_2345del (p.(Asp778_Lys781del))
ISCN -
DB-ID AFG3L2_000079
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AFG3L2 NM_006796.2 ?/. - c.2334_2345del r.(?) p.(Asp778_Lys781del)
TUBB6 NM_032525.1 ?/. - c.*3489_*3500del r.(=) p.(=)


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