Variant #0000292107 (NC_000001.10:g.11854874C>A, NM_005957.4:c.1078G>T (MTHFR))

Chromosome 1
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.11854874C>A
DNA change (hg38) g.11794817C>A
Published as MTHFR(NM_005957.4):c.1078G>T (p.E360*)
ISCN -
DB-ID MTHFR_000018
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN6 NM_001286.3 +/. - c.-11446C>A r.(?) p.(=)
MTHFR NM_005957.4 +/. - c.1078G>T r.(?) p.(Glu360Ter)


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