Variant #0000716721 (NC_000001.10:g.11852411C>A, NM_005957.4:c.1556G>T (MTHFR))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.11852411C>A
DNA change (hg38) -
Published as MTHFR(NM_005957.4):c.1556G>T (p.R519L), MTHFR(NM_005957.5):c.1556G>T (p.R519L)
ISCN -
DB-ID MTHFR_000079 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) 0.00054 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN6 NM_001286.3 ?/. - c.-13909C>A r.(?) p.(=)
MTHFR NM_005957.4 ?/. - c.1556G>T r.(?) p.(Arg519Leu)


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