Variant #0000856900 (NC_000001.10:g.11851003G>C, NC_000001.10(NM_005957.4):c.1753-48C>G (MTHFR))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.11851003G>C
DNA change (hg38) -
Published as MTHFR(NM_001330358.1):c.1876-48C>G
ISCN -
DB-ID MTHFR_000091
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) 0.26114 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN6 NM_001286.3 -/. - c.-15317G>C r.(?) p.(=)
MTHFR NM_005957.4 -/. - c.1753-48C>G r.(=) p.(=)


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