Variant #0001042031 (NC_000017.10:g.57771081T>C, NC_000017.10(NM_004859.3):c.4904-8T>C (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.57771081T>C
DNA change (hg38) -
Published as CLTC(NM_004859.4):c.4904-8T>C
ISCN -
DB-ID CLTC_000061
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
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.4904-8T>C r.(=) p.(=)
PTRH2 NM_016077.3 -?/. - c.*3719A>G r.(=) p.(=)
VMP1 NM_030938.3 -?/. - c.-14055T>C r.(?) p.(=)


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