Variant #0000877069 (NC_000007.13:g.124491951T>C, NM_015450.2:c.924A>G (POT1))

Chromosome 7
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.124491951T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID POT1_000013 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs34398311
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00618 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-08-23 12:42:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POT1 NM_015450.2 -/. - c.924A>G r.(?) p.(Gln308=)


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