Variant #0000911516 (NC_000002.11:g.207636605G>A, NC_000002.11(NM_001136194.1):c.991-13G>A (FASTKD2))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.207636605G>A
DNA change (hg38) -
Published as FASTKD2(NM_014929.4):c.991-13G>A
ISCN -
DB-ID FASTKD2_000014
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) 0.00356 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FASTKD2 NM_001136194.1 -/. - c.991-13G>A r.(=) p.(=)
FASTKD2 NM_014929.3 -/. - c.991-13G>A r.(=) p.(=)


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