Variant #0000653656 (NC_000001.10:g.150483951C>T, NM_004425.3:c.727C>T (ECM1))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.150483951C>T
DNA change (hg38) g.150511475C>T
Published as ECM1(NM_001202858.1):c.808C>T (p.R270*)
ISCN -
DB-ID ECM1_000018
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) 0 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ECM1 NM_004425.3 +/. - c.727C>T r.(?) p.(Arg243Ter)
TARS2 NM_025150.3 +/. - c.*4411C>T r.(=) p.(=)


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