Variant #0000503077 (NC_000001.10:g.150479525C>T, NM_004425.3:c.-1161C>T (ECM1))

Chromosome 1
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.150479525C>T
DNA change (hg38) g.150507049C>T
Published as TARS2(NM_025150.4):c.2142C>T (p.A714=)
ISCN -
DB-ID ECM1_000014
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
ECM1 NM_004425.3 -?/. - c.-1161C>T r.(?) p.(=)
TARS2 NM_025150.3 -?/. - c.2142C>T r.(?) p.(Ala714=)


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