Variant #0000726552 (NC_000017.10:g.57775279C>T, NM_004859.3:c.*4066C>T (CLTC))

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.57775279C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CLTC_000025
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) 0.00417 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-02-08 18:36:18 +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     
CLTC NM_004859.3 -?/. - c.*4066C>T r.(=) p.(=)
PTRH2 NM_016077.3 -?/. - c.61G>A r.(?) p.(Val21Ile)
VMP1 NM_030938.3 -?/. - c.-9857C>T r.(?) p.(=)


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