Variant #0000680524 (NC_000016.9:g.3024324C>T, NM_172229.2:c.*6303C>T (KREMEN2))

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.3024324C>T
DNA change (hg38) -
Published as PKMYT1(NM_182687.2):c.1074G>A (p.V358=)
ISCN -
DB-ID KREMEN2_000007
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PKMYT1 NM_004203.4 -?/. - c.1074G>A r.(?) p.(Val358=)
PAQR4 NM_152341.3 -?/. - c.*2375C>T r.(=) p.(=)
KREMEN2 NM_172229.2 -?/. - c.*6303C>T r.(=) p.(=)


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