Variant #0000557848 (NC_000016.9:g.3014990C>A, NM_172229.2:c.225C>A (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.3014990C>A
DNA change (hg38) g.2964989C>A
Published as KREMEN2(NM_001253725.1):c.225C>A (p.(Ser75Arg))
ISCN -
DB-ID KREMEN2_000001
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) 0.01755 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PKMYT1 NM_004203.4 -?/. - c.*7964G>T r.(=) p.(=)
PAQR4 NM_152341.3 -?/. - c.-4686C>A r.(?) p.(=)
KREMEN2 NM_172229.2 -?/. - c.225C>A r.(?) p.(Ser75Arg)


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