Variant #0000528761 (NC_000006.11:g.35478765_35478773dup, NM_003322.3:c.378_386dup (TULP1))

Chromosome 6
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.35478765_35478773dup
DNA change (hg38) g.35510988_35510996dup
Published as TULP1(NM_003322.5):c.378_386dupGGACGAGGA (p.D127_E129dup)
ISCN -
DB-ID TULP1_000087
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
TULP1 NM_003322.3 -/. - c.378_386dup r.(?) p.(Asp127_Glu129dup)


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