Variant #0000330564 (NC_000005.9:g.140077210G>C, NM_012208.3:c.1254G>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.140077210G>C
DNA change (hg38) g.140697625G>C
Published as HARS2(NM_001278731.1):c.1179G>C (p.(Gln393His)), HARS2(NM_012208.3):c.1254G>C (p.Q418H)
ISCN -
DB-ID HARS2_000003 See all 2 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) 8.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HARS2 NM_012208.3 -?/. - c.1254G>C r.(?) p.(Gln418His)
ZMAT2 NM_144723.1 -?/. - c.-2836G>C r.(?) p.(=)


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