Variant #0000982602 (NC_000017.10:g.48263369C>T, NM_000088.3:c.4018G>A (COL1A1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48263369C>T
DNA change (hg38) -
Published as COL1A1(NM_000088.3):c.4018G>A (p.G1340S), COL1A1(NM_000088.4):c.4018G>A (p.(Gly1340Ser))
ISCN -
DB-ID COL1A1_000539 See all 6 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) 0.00066 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     

Predicted     

Legacy protein change     
COL1A1 NM_000088.3 -?/. - c.4018G>A r.(?) p.(Gly1340Ser) - -


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