Variant #0000859782 (NC_000005.9:g.140075089T>C, NC_000005.9(NM_012208.3):c.400-4T>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.140075089T>C
DNA change (hg38) -
Published as HARS2(NM_001363535.1):c.418-4T>C
ISCN -
DB-ID ZMAT2_000012
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HARS2 NM_012208.3 -?/. - c.400-4T>C r.spl? p.?
ZMAT2 NM_144723.1 -?/. - c.-4957T>C r.(?) p.(=)


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