Variant #0000329757 (NC_000003.11:g.186953480C>T, NC_000003.11(NM_001879.5):c.1303+5789G>A (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.186953480C>T
DNA change (hg38) g.187235692C>T
Published as MASP1(NM_139125.3):c.2179G>A (p.(Glu727Lys))
ISCN -
DB-ID MASP1_000008
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) 0.00066 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 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+5789G>A r.(=) p.(=)
MASP1 NM_139125.3 ?/. - c.2179G>A r.(?) p.(Glu727Lys)


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