Variant #0000981907 (NC_000016.9:g.4431315C>T, NC_000016.9(NM_024535.4):c.785+6672G>A (CORO7))

Chromosome 16
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.4431315C>T
DNA change (hg38) -
Published as VASN(NM_138440.3):c.437C>T (p.(Thr146Met))
ISCN -
DB-ID CORO7_000031
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) 0.00348 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CORO7-PAM16 NM_001201479.1 -?/. - c.785+6672G>A r.(=) p.(=)
PAM16 NM_016069.9 -?/. - c.-30080G>A r.(?) p.(=)
CORO7 NM_024535.4 -?/. - c.785+6672G>A r.(=) p.(=)
VASN NM_138440.2 -?/. - c.437C>T r.(?) p.(Thr146Met)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.