Variant #0000604703 (NC_000001.10:g.11861234G>C, NM_005957.4:c.459C>G (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.11861234G>C
DNA change (hg38) g.11801177G>C
Published as MTHFR(NM_001330358.2):c.582C>G (p.I194M)
ISCN -
DB-ID MTHFR_000056
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) 0.00011 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 14:54:23 +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     
CLCN6 NM_001286.3 +/. - c.-5086G>C r.(?) p.(=)
MTHFR NM_005957.4 +/. - c.459C>G r.(?) p.(Ile153Met)


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