Variant #0000718838 (NC_000002.11:g.47135009del, NM_020458.2:c.-33672del (TTC7A))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47135009del
DNA change (hg38) -
Published as MCFD2(NM_001171508.2):c.249delT (p.D83Efs*9)
ISCN -
DB-ID MCFD2_000001 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTC7A NM_020458.2 +/. - c.-33672del r.(?) p.(=)
MCFD2 NM_139279.5 +/. - c.249del r.(?) p.(Asp83GlufsTer9)


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