Variant #0001054390 (NC_000012.11:g.58144665C>T, NM_138396.5:c.-4647C>T (MARCH9))

Chromosome 12
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.58144665C>T
DNA change (hg38) -
Published as CDK4(NM_000075.4):c.522+41G>A (None)
ISCN -
DB-ID CDK4_000016
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) 0.35521 View details
Owner VKGL-NL_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDK4 NM_000075.3 -/. - c.522+41G>A r.(=) p.(=)
TSPAN31 NM_005981.3 -/. - c.*3592C>T r.(=) p.(=)
MARCH9 NM_138396.5 -/. - c.-4647C>T r.(?) p.(=)


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