Variant #0000716722 (NC_000001.10:g.11854476T>G, NM_005957.4:c.1286A>C (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.11854476T>G
DNA change (hg38) -
Published as MTHFR(NM_001330358.1):c.1409A>C (p.E470A), MTHFR(NM_005957.4):c.1286A>C (p.E429A), MTHFR(NM_005957.5):c.1286A>C (p.E429A, p.(Glu429Ala))
ISCN -
DB-ID MTHFR_000016 See all 6 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) 0.29019 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-04-19 20:20:39 +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.-11844T>G r.(?) p.(=)
MTHFR NM_005957.4 -/. - c.1286A>C r.(?) p.(Glu429Ala)


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