Variant #0000556926 (NC_000016.9:g.16263662G>T, NM_001171.5:c.2836C>A (ABCC6))

Chromosome 16
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.16263662G>T
DNA change (hg38) g.16169805G>T
Published as ABCC6(NM_001171.5):c.2836C>A (p.(Leu946Ile)), ABCC6(NM_001171.6):c.2836C>A (p.L946I), ABCC6(NM_001351800.1):c.2494C>A (p.L832I)
ISCN -
DB-ID ABCC6_000111 See all 19 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) 0.01649 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCC6 NM_001171.5 -?/. - c.2836C>A r.(?) p.(Leu946Ile)


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