Variant #0000911723 (NC_000002.11:g.47168774C>G, NM_020458.2:c.94C>G (TTC7A))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47168774C>G
DNA change (hg38) -
Published as TTC7A(NM_001288951.1):c.94C>G (p.L32V), TTC7A(NM_020458.4):c.94C>G (p.L32V)
ISCN -
DB-ID TTC7A_000002 See all 2 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) 0.00249 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 2023-01-11 15:44:22 +01:00 (CET)
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.94C>G r.(?) p.(Leu32Val)
MCFD2 NM_139279.5 -?/. - c.-25919G>C r.(?) p.(=)


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