Variant #0000265243 (NC_000011.9:g.6644270G>A, NM_000391.3:c.-3639C>T (TPP1))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6644270G>A
DNA change (hg38) g.6623039G>A
Published as DCHS1(NM_003737.2):c.8640C>T (p.G2880=), DCHS1(NM_003737.4):c.8637C>T (p.S2879=, p.(Ser2879=))
ISCN -
DB-ID DCHS1_000019 See all 3 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPP1 NM_000391.3 -/. - c.-3639C>T r.(?) p.(=)
DCHS1 NM_003737.2 -/. - c.8637C>T r.(?) p.(=)


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