Variant #0000311065 (NC_000006.11:g.35478756_35478779del, NM_003322.3:c.371_394del (TULP1))

Chromosome 6
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.35478756_35478779del
DNA change (hg38) g.35510979_35511002del
Published as TULP1(NM_003322.5):c.371_394delACGAGGAGGACGAGGAAGAGGAGG (p.D124_E131del), TULP1(NM_003322.6):c.371_394delACGAGGAGGACGAGGAAGAGGAGG (p.D124_E131del)
ISCN -
DB-ID TULP1_000058 See all 7 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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TULP1 NM_003322.3 ?/. - c.371_394del r.(?) p.(Asp124_Glu131del)


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