Variant #0000563012 (NC_000017.10:g.73513185C>A, NC_000017.10(NM_207346.2):c.285+32C>A (TSEN54))

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.73513185C>A
DNA change (hg38) g.75517104C>A
Published as TSEN54(NM_207346.2):c.285+32C>A, TSEN54(NM_207346.3):c.285+32C>A
ISCN -
DB-ID KIAA0195_000025 See all 2 reported entries
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) 0.6023 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0195 NM_014738.4 -/. - c.*17770C>A r.(=) p.(=)
CASKIN2 NM_020753.3 -/. - c.-2108G>T r.(?) p.(=)
TSEN54 NM_207346.2 -/. - c.285+32C>A r.(=) p.(=)


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