Variant #0000350459 (NC_000011.9:g.6644059C>G, NM_000391.3:c.-3428G>C (TPP1))

Chromosome 11
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.6644059C>G
DNA change (hg38) g.6622828C>G
Published as DCHS1(NM_003737.4):c.8848G>C (p.V2950L)
ISCN -
DB-ID DCHS1_000071 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPP1 NM_000391.3 ?/. - c.-3428G>C r.(?) p.(=)
DCHS1 NM_003737.2 ?/. - c.8848G>C r.(?) p.(Val2950Leu)


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