Variant #0000538410 (NC_000009.11:g.713452G>C, NM_015158.3:c.2686G>C (KANK1))

Chromosome 9
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.713452G>C
DNA change (hg38) g.713452G>C
Published as KANK1(NM_001256876.1):c.2686G>C (p.(Gly896Arg)), KANK1(NM_001256877.2):c.2686G>C (p.G896R)
ISCN -
DB-ID KANK1_000044 See all 2 reported entries
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) 0.00019 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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KANK1 NM_015158.3 -?/. - c.2686G>C r.(?) p.(Gly896Arg)


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