Variant #0000913920 (NC_000012.11:g.58145379T>C, NM_138396.5:c.-3933T>C (MARCH9))

Chromosome 12
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.58145379T>C
DNA change (hg38) -
Published as CDK4(NM_000075.3):c.122A>G (p.(Asn41Ser))
ISCN -
DB-ID CDK4_000009
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) 0.00012 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 2023-01-11 15:44:22 +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.122A>G r.(?) p.(Asn41Ser)
TSPAN31 NM_005981.3 ?/. - c.*4306T>C r.(=) p.(=)
MARCH9 NM_138396.5 ?/. - c.-3933T>C r.(?) p.(=)


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