Variant #0000960406 (NC_000001.10:g.11907243C>T, NM_005957.4:c.-41312G>A (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.11907243C>T
DNA change (hg38) -
Published as NPPA(NM_006172.3):c.377G>A (p.(Arg126Gln))
ISCN -
DB-ID MTHFR_000117
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) 9.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN6 NM_001286.3 ?/. - c.*6963C>T r.(=) p.(=)
MTHFR NM_005957.4 ?/. - c.-41312G>A r.(?) p.(=)
NPPA NM_006172.3 ?/. - c.377G>A r.(?) p.(Arg126Gln)
NPPA-AS1 NR_037806.1 ?/. - n.1480-248C>T r.(?) -


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