Variant #0000680523 (NC_000016.9:g.3024011C>G, NM_172229.2:c.*5990C>G (KREMEN2))

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.3024011C>G
DNA change (hg38) -
Published as PKMYT1(NM_182687.2):c.1300G>C (p.D434H)
ISCN -
DB-ID KREMEN2_000006
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 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.1300G>C r.(?) p.(Asp434His)
PAQR4 NM_152341.3 ?/. - c.*2062C>G r.(=) p.(=)
KREMEN2 NM_172229.2 ?/. - c.*5990C>G r.(=) p.(=)


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