Variant #0000863615 (NC_000014.8:g.64898338_64898339del, NM_005956.3:c.1400_1401del (MTHFD1))

Chromosome 14
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.64898338_64898339del
DNA change (hg38) -
Published as MTHFD1(NM_005956.4):c.1400_1401delAA (p.E467Afs*10)
ISCN -
DB-ID MTHFD1_000029
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 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 2022-05-09 15:51:19 +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     
MTHFD1 NM_005956.3 +/. - c.1400_1401del r.(?) p.(Glu467Alafs*10)


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