Variant #0000805210 (NC_000011.9:g.61165270G>A, NM_001173990.2:c.254G>A (TMEM216))

Chromosome 11
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.61165270G>A
DNA change (hg38) -
Published as TMEM216(NM_001330285.1):c.71G>A (p.R24Q)
ISCN -
DB-ID CPSF7_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) 2.0E-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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM216 NM_001173990.2 ?/. - c.254G>A r.(?) p.(Arg85Gln)
CPSF7 NM_024811.3 ?/. - c.*6912C>T r.(=) p.(=)


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