Variant #0000325524 (NC_000017.10:g.57775000G>C, NM_004859.3:c.*3787G>C (CLTC))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.57775000G>C
DNA change (hg38) g.59697639G>C
Published as PTRH2(NM_016077.3):c.340C>G (p.(Pro114Ala))
ISCN -
DB-ID PTRH2_000001
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLTC NM_004859.3 ?/. - c.*3787G>C r.(=) p.(=)
PTRH2 NM_016077.3 ?/. - c.340C>G r.(?) p.(Pro114Ala)
VMP1 NM_030938.3 ?/. - c.-10136G>C r.(?) p.(=)


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