Variant #0000524442 (NC_000005.9:g.140050894G>C, NM_012208.3:c.-20340G>C (HARS2))

Chromosome 5
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.140050894G>C
DNA change (hg38) g.140671309G>C
Published as DND1(NM_194249.2):c.1046C>G (p.(Thr349Ser))
ISCN -
DB-ID DND1_000001
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HARS NM_002109.3 -?/. - c.*2948C>G r.(=) p.(=)
HARS2 NM_012208.3 -?/. - c.-20340G>C r.(?) p.(=)
WDR55 NM_017706.4 -?/. - c.*1655G>C r.(=) p.(=)
DND1 NM_194249.2 -?/. - c.1046C>G r.(?) p.(Thr349Ser)


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