Variant #0000799422 (NC_000001.10:g.55199341del, NM_001039464.2:c.*23481del (MROH7))

Chromosome 1
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.55199341del
DNA change (hg38) -
Published as TTC4(NM_004623.4):c.936delC (p.S313Lfs*4)
ISCN -
DB-ID TTC4_000005
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MROH7 NM_001039464.2 ?/. - c.*23481del r.(?) p.(=)
TTC4 NM_004623.4 ?/. - c.936del r.(?) p.(Ser313Leufs*4)


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