Variant #0000622433 (NC_000010.10:g.79397284_79397286dup, NM_001014797.2:c.135_137dup (KCNMA1))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.79397284_79397286dup
DNA change (hg38) g.77637526_77637528dup
Published as KCNMA1(NM_001014797.3):c.135_137dupCTC (p.S60dup), KCNMA1(NM_001322830.2):c.135_137dupCTC (p.S60dup)
ISCN -
DB-ID KCNMA1_000092 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
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     
KCNMA1 NM_001014797.2 -/. - c.135_137dup r.(?) p.(Ser60dup)


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