Variant #0000516080 (NC_000002.11:g.47168856C>G, NM_020458.2:c.176C>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.47168856C>G
DNA change (hg38) g.46941717C>G
Published as TTC7A(NM_001288951.1):c.176C>G (p.P59R), TTC7A(NM_020458.2):c.176C>G (p.(Pro59Arg)), TTC7A(NM_020458.4):c.176C>G (p.P59R)
ISCN -
DB-ID TTC7A_000004 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) 0.00349 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTC7A NM_020458.2 -?/. - c.176C>G r.(?) p.(Pro59Arg)
MCFD2 NM_139279.5 -?/. - c.-26001G>C r.(?) p.(=)


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