Variant #0000922925 (NC_000001.10:g.11907492A>G, NM_005957.4:c.-41561T>C (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.11907492A>G
DNA change (hg38) -
Published as NPPA(NM_006172.4):c.128T>C (p.L43S)
ISCN -
DB-ID MTHFR_000104 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) 1.0E-5 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 2023-04-16 21:50:28 +02:00 (CEST)
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.*7212A>G r.(=) p.(=)
MTHFR NM_005957.4 ?/. - c.-41561T>C r.(?) p.(=)
NPPA NM_006172.3 ?/. - c.128T>C r.(?) p.(Leu43Ser)
NPPA-AS1 NR_037806.1 ?/. - n.1481A>G r.(?) -


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