Variant #0000275894 (NC_000001.10:g.150484317C>T, NC_000001.10(NM_004425.3):c.1083+10C>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.150484317C>T
DNA change (hg38) g.150511841C>T
Published as ECM1(NM_001202858.1):c.1164+10C>T
ISCN -
DB-ID ECM1_000007
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) 0.00391 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 2018-01-15 20:58:59 +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.1083+10C>T r.(=) p.(=)
TARS2 NM_025150.3 -?/. - c.*4777C>T r.(=) p.(=)


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