Variant #0000806014 (NC_000013.10:g.110864822A>G, NM_001845.4:c.329T>C (COL4A1))

Chromosome 13
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.110864822A>G
DNA change (hg38) -
Published as COL4A1(NM_001845.5):c.329T>C (p.I110T), COL4A1(NM_001845.6):c.329T>C (p.I110T)
ISCN -
DB-ID COL4A1_000243 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) 0.00022 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     
COL4A1 NM_001845.4 ?/. - c.329T>C r.(?) p.(Ile110Thr)


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