Variant #0000291527 (NC_000003.11:g.186953906G>T, NC_000003.11(NM_001879.5):c.1303+5363C>A (MASP1))

Chromosome 3
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.186953906G>T
DNA change (hg38) g.187236118G>T
Published as MASP1(NM_139125.3):c.1753C>A (p.H585N)
ISCN -
DB-ID MASP1_000009
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) 2.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MASP1 NM_001879.5 -?/. - c.1303+5363C>A r.(=) p.(=)
MASP1 NM_139125.3 -?/. - c.1753C>A r.(?) p.(His585Asn)


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