Variant #0001035843 (NC_000006.11:g.5265216_5265218dup, NC_000006.11(NM_006567.3):c.-22+3323_-22+3325dup (FARS2))

Chromosome 6
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.5265216_5265218dup
DNA change (hg38) -
Published as FARS2(NM_001374879.1):c.-110-7_-110-5dup
ISCN -
DB-ID FARS2_000040
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 2025-05-05 21:14:00 +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     
PPP1R3G NM_001145115.1 ?/. - c.*178420_*178422dup r.(=) p.(=)
FARS2 NM_006567.3 ?/. - c.-22+3323_-22+3325dup r.(=) p.(=)
LYRM4 NM_020408.4 ?/. - c.-4240_-4238dup r.(?) p.(=)


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