Variant #0000502663 (NC_000001.10:g.11854498C>T, NM_005957.4:c.1264G>A (MTHFR))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.11854498C>T
DNA change (hg38) g.11794441C>T
Published as MTHFR(NM_001330358.1):c.1387G>A (p.G463R), MTHFR(NM_005957.5):c.1264G>A (p.G422R)
ISCN -
DB-ID MTHFR_000041 See all 2 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) 0.00063 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.-11822C>T r.(?) p.(=)
MTHFR NM_005957.4 -?/. - c.1264G>A r.(?) p.(Gly422Arg)


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