Variant #0000856902 (NC_000001.10:g.11854034T>C, NM_005957.4:c.1460A>G (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.11854034T>C
DNA change (hg38) -
Published as MTHFR(NM_005957.4):c.1460A>G (p.N487S)
ISCN -
DB-ID MTHFR_000093
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +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.-12286T>C r.(?) p.(=)
MTHFR NM_005957.4 -?/. - c.1460A>G r.(?) p.(Asn487Ser)


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