Variant #0000882715 (NC_000001.10:g.11850835_11850838dup, NM_005957.4:c.1871_1874dup (MTHFR))

Chromosome 1
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.11850835_11850838dup
DNA change (hg38) -
Published as MTHFR(NM_001330358.1):c.1994_1997dupATGA (p.D666Efs*2)
ISCN -
DB-ID MTHFR_000107
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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN6 NM_001286.3 ?/. - c.-15485_-15482dup r.(?) p.(=)
MTHFR NM_005957.4 ?/. - c.1871_1874dup r.(?) p.(Asp625Glufs*2)


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