Variant #0000620366 (NC_000001.10:g.11907328C>T, NM_005957.4:c.-41397G>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.11907328C>T
DNA change (hg38) g.11847271C>T
Published as NPPA(NM_006172.4):c.292G>A (p.G98R)
ISCN -
DB-ID MTHFR_000061
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-06 12:43:26 +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.*7048C>T r.(=) p.(=)
MTHFR NM_005957.4 -?/. - c.-41397G>A r.(?) p.(=)
NPPA NM_006172.3 -?/. - c.292G>A r.(?) p.(Gly98Arg)
NPPA-AS1 NR_037806.1 -?/. - n.1480-163C>T r.(?) -


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