Variant #0000914750 (NC_000017.10:g.18161744C>T, NC_000017.10(NM_002018.3):c.63+198G>A (FLII))

Chromosome 17
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.18161744C>T
DNA change (hg38) -
Published as FLII(NM_001256264.2):c.30+17G>A
ISCN -
DB-ID FLII_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) 0.24681 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     
FLII NM_002018.3 -/. - c.63+198G>A r.(=) p.(=)
LLGL1 NM_004140.3 -/. - c.*14524C>T r.(=) p.(=)
SMCR7 NM_139162.3 -/. - c.-2315C>T r.(?) p.(=)


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