Variant #0000316683 (NC_000011.9:g.61165741G>C, NC_000011.9(NM_001173990.2):c.432-1G>C (TMEM216))

Chromosome 11
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.61165741G>C
DNA change (hg38) g.61398269G>C
Published as TMEM216(NM_001173990.3):c.432-1G>C, TMEM216(NM_001173991.2):c.440G>C (p.R147T)
ISCN -
DB-ID TMEM216_000016 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) 0.83031 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM216 NM_001173990.2 -/. - c.432-1G>C r.spl? p.?
CPSF7 NM_024811.3 -/. - c.*6441C>G r.(=) p.(=)


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