Variant #0000861544 (NC_000009.11:g.136333062G>A, NM_017586.3:c.340G>A (CACFD1))

Chromosome 9
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.136333062G>A
DNA change (hg38) -
Published as CACFD1(NM_001135775.2):c.214G>A (p.(Val72Ile))
ISCN -
DB-ID CACFD1_000004
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC2A6 NM_017585.3 -?/. - c.*4081C>T r.(=) p.(=)
CACFD1 NM_017586.3 -?/. - c.340G>A r.(?) p.(Val114Ile)


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