Variant #0000516085 (NC_000002.11:g.47220630G>A, NM_020458.2:c.806G>A (TTC7A))

Chromosome 2
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.47220630G>A
DNA change (hg38) g.46993491G>A
Published as TTC7A(NM_001288951.1):c.806G>A (p.R269Q), TTC7A(NM_001288951.2):c.806G>A (p.R269Q)
ISCN -
DB-ID TTC7A_000030 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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTC7A NM_020458.2 ?/. - c.806G>A r.(?) p.(Arg269Gln)


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