Variant #0000292111 (NC_000001.10:g.11854085_11854086delinsAG, NM_005957.4:c.1408_1409delinsCT (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.11854085_11854086delinsAG
DNA change (hg38) g.11794028_11794029delinsAG
Published as MTHFR(NM_005957.4):c.1408_1409delGAinsCT (p.E470L)
ISCN -
DB-ID MTHFR_000013
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLCN6 NM_001286.3 ?/. - c.-12235_-12234delinsAG r.(?) p.(=)
MTHFR NM_005957.4 ?/. - c.1408_1409delinsCT r.(?) p.(Glu470Leu)


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