Variant #0000990160 (NC_000001.10:g.11897186_11897214dup, NM_005957.4:c.-31276_-31248dup (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.11897186_11897214dup
DNA change (hg38) -
Published as CLCN6(NM_001286.3):c.2111_2138+1dupACCTCCTGCAGCAGATGCTGGAAAGGAGG (p.?)
ISCN -
DB-ID MTHFR_000130
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +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.2111_2138+1dup r.spl? p.?
MTHFR NM_005957.4 ?/. - c.-31276_-31248dup r.(?) p.(=)
NPPA NM_006172.3 ?/. - c.*8859_*8887dup r.(=) p.(=)


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