Variant #0000287979 (NC_000001.10:g.24194776T>C, NM_000147.4:c.1A>G (FUCA1))

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.24194776T>C
DNA change (hg38) g.23868286T>C
Published as FUCA1(NM_000147.4):c.1A>G (p.M1?)
ISCN -
DB-ID FUCA1_000009
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) 0.00011 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-04 09:22:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FUCA1 NM_000147.4 ?/. - c.1A>G r.(?) p.(Met1?)
CNR2 NM_001841.2 ?/. - c.*6249A>G r.(=) p.(=)


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