Variant #0001045896 (NC_000003.11:g.186953672C>A, NC_000003.11(NM_001879.5):c.1303+5597G>T (MASP1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.186953672C>A
DNA change (hg38) -
Published as MASP1(NM_139125.4):c.1987G>T (p.D663Y)
ISCN -
DB-ID MASP1_000040 See all 2 reported entries
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MASP1 NM_001879.5 +?/. - c.1303+5597G>T r.(=) p.(=)
MASP1 NM_139125.3 +?/. - c.1987G>T r.(?) p.(Asp663Tyr)


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