Variant #0000316753 (NC_000017.10:g.73494391G>T, NM_014738.4:c.3625G>T (KIAA0195))

Chromosome 17
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.73494391G>T
DNA change (hg38) g.75498310G>T
Published as TMEM94(NM_014738.5):c.3625G>T (p.V1209F), TMEM94(NM_014738.6):c.3625G>T (p.(Val1209Phe))
ISCN -
DB-ID KIAA0195_000002 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) 0.00077 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 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0195 NM_014738.4 -?/. - c.3625G>T r.(?) p.(Val1209Phe)
CASKIN2 NM_020753.3 -?/. - c.*2770C>A r.(=) p.(=)


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