Variant #0000928605 (NC_000002.11:g.47168838G>C, NM_020458.2:c.158G>C (TTC7A))

Chromosome 2
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.47168838G>C
DNA change (hg38) -
Published as TTC7A(NM_020458.4):c.158G>C (p.S53T)
ISCN -
DB-ID TTC7A_000003
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) 0.00247 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-07-07 10:10:56 +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     
TTC7A NM_020458.2 -/. - c.158G>C r.(?) p.(Ser53Thr)
MCFD2 NM_139279.5 -/. - c.-25983C>G r.(?) p.(=)


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