Variant #0000604706 (NC_000001.10:g.11907269C>T, NM_005957.4:c.-41338G>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.11907269C>T
DNA change (hg38) g.11847212C>T
Published as -
ISCN -
DB-ID MTHFR_000060
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) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.*6989C>T r.(=) p.(=)
MTHFR NM_005957.4 -?/. - c.-41338G>A r.(?) p.(=)
NPPA NM_006172.3 -?/. - c.351G>A r.(?) p.(Ala117=)
NPPA-AS1 NR_037806.1 -?/. - n.1480-222C>T r.(?) -


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