Variant #0000552826 (NC_000014.8:g.64911444A>G, NM_005956.3:c.2170A>G (MTHFD1))

Chromosome 14
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.64911444A>G
DNA change (hg38) g.64444726A>G
Published as MTHFD1(NM_005956.4):c.2170A>G (p.I724V)
ISCN -
DB-ID AKAP5_000001
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) 3.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
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     
ZBTB1 NM_001123329.1 -?/. - c.-60239A>G r.(?) p.(=)
AKAP5 NM_004857.3 -?/. - c.-21151A>G r.(?) p.(=)
MTHFD1 NM_005956.3 -?/. - c.2170A>G r.(?) p.(Ile724Val)
ZBTB25 NM_006977.2 -?/. - c.*42197T>C r.(=) p.(=)


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