Variant #0000725797 (NC_000016.9:g.4432503G>A, NC_000016.9(NM_024535.4):c.785+5484C>T (CORO7))

Chromosome 16
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.4432503G>A
DNA change (hg38) -
Published as VASN(NM_138440.3):c.1625G>A (p.R542Q)
ISCN -
DB-ID CORO7_000015
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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     
CORO7-PAM16 NM_001201479.1 ?/. - c.785+5484C>T r.(=) p.(=)
PAM16 NM_016069.9 ?/. - c.-31268C>T r.(?) p.(=)
CORO7 NM_024535.4 ?/. - c.785+5484C>T r.(=) p.(=)
VASN NM_138440.2 ?/. - c.1625G>A r.(?) p.(Arg542Gln)


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