Variant #0000292115 (NC_000001.10:g.11852412G>A, NM_005957.4:c.1555C>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.11852412G>A
DNA change (hg38) g.11792355G>A
Published as MTHFR(NM_001330358.1):c.1678C>T (p.R560C), MTHFR(NM_005957.5):c.1555C>T (p.R519C)
ISCN -
DB-ID MTHFR_000008 See all 3 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) 0.00066 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN6 NM_001286.3 ?/. - c.-13908G>A r.(?) p.(=)
MTHFR NM_005957.4 ?/. - c.1555C>T r.(?) p.(Arg519Cys)


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