Variant #0000848252 (NC_000001.10:g.11850962_11850981del, NC_000001.10(NM_005957.4):c.1753-22_1753-3del (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.11850962_11850981del
DNA change (hg38) -
Published as MTHFR(NM_001330358.1):c.1876-22_1876-3delGTGCGGGGGTATGTGTGTGT, MTHFR(NM_005957.4):c.1753-22_1753-3delGTGCGGGGGTATGTGTGTGT
ISCN -
DB-ID MTHFR_000090
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) Retrieve
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 15:40:45 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN6 NM_001286.3 ?/. - c.-15358_-15339del r.(?) p.(=)
MTHFR NM_005957.4 ?/. - c.1753-22_1753-3del r.spl? p.?


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