Variant #0000340883 (NC_000001.10:g.11854457G>A, NM_005957.4:c.1305C>T (MTHFR))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.11854457G>A
DNA change (hg38) g.11794400G>A
Published as MTHFR(NM_005957.4):c.1305C>T (p.F435=), MTHFR(NM_005957.5):c.1305C>T (p.F435=)
ISCN -
DB-ID MTHFR_000015 See all 4 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) 0.97553 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN6 NM_001286.3 -/. - c.-11863G>A r.(?) p.(=)
MTHFR NM_005957.4 -/. - c.1305C>T r.(?) p.(Phe435=)


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