Variant #0000612161 (NC_000009.11:g.73236156_73236159del, NC_000009.11(NM_206945.3):c.1351-876_1351-873del (TRPM3))

Chromosome 9
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.73236156_73236159del
DNA change (hg38) g.70621240_70621243del
Published as TRPM3(NM_001007471.3):c.1803+3_1803+6delAAGT
ISCN -
DB-ID TRPM3_000017
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRPM3 NM_206945.3 ?/. - c.1351-876_1351-873del r.(=) p.(=)


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