Variant #0000851321 (NC_000006.11:g.75890945_75890946dup, NC_000006.11(NM_004370.5):c.1892-8_1892-7dup (COL12A1))

Chromosome 6
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.75890945_75890946dup
DNA change (hg38) -
Published as COL12A1(NM_004370.5):c.1892-8_1892-7dup (p.(=)), COL12A1(NM_004370.5):c.1892-8_1892-7dupTT, COL12A1(NM_004370.6):c.1892-8_1892-7dupTT
ISCN -
DB-ID COL12A1_000082 See all 4 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL12A1 NM_004370.5 -/. - c.1892-8_1892-7dup r.(=) p.(=)


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