Variant #0001031102 (NC_000001.10:g.11883810A>G, NM_005957.4:c.-17879T>C (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.11883810A>G
DNA change (hg38) -
Published as CLCN6(NM_001286.5):c.500A>G (p.(Asn167Ser))
ISCN -
DB-ID MTHFR_000140
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) 3.0E-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 2025-05-05 21:14:00 +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.500A>G r.(?) p.(Asn167Ser)
MTHFR NM_005957.4 -?/. - c.-17879T>C r.(?) p.(=)


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