Variant #0000518709 (NC_000003.11:g.186954152G>A, NC_000003.11(NM_001879.5):c.1303+5117C>T (MASP1))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.186954152G>A
DNA change (hg38) g.187236364G>A
Published as MASP1(NM_139125.3):c.1507C>T (p.R503C, p.(Arg503Cys))
ISCN -
DB-ID MASP1_000026 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) 0.00043 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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+5117C>T r.(=) p.(=)
MASP1 NM_139125.3 ?/. - c.1507C>T r.(?) p.(Arg503Cys)


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