Variant #0000653606 (NC_000001.10:g.11907282C>G, NM_005957.4:c.-41351G>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.11907282C>G
DNA change (hg38) g.11847225C>G
Published as NPPA(NM_006172.4):c.338G>C (p.S113T)
ISCN -
DB-ID MTHFR_000066
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-03-23 16:13:27 +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.*7002C>G r.(=) p.(=)
MTHFR NM_005957.4 ?/. - c.-41351G>C r.(?) p.(=)
NPPA NM_006172.3 ?/. - c.338G>C r.(?) p.(Ser113Thr)
NPPA-AS1 NR_037806.1 ?/. - n.1480-209C>G r.(?) -


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