Variant #0000273827 (NC_000010.10:g.105793763C>T, COL17A1(NM_000494.3):c.4096G>A)

Chromosome 10
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.105793763C>T
DNA change (hg38) g.104034005C>T
Published as COL17A1(NM_000494.4):c.4096G>A (p.D1366N)
ISCN -
DB-ID COL17A1_000005
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL17A1 NM_000494.3 -?/. - c.4096G>A r.(?) p.(Asp1366Asn)
SLK NM_014720.2 -?/. - c.*8285C>T r.(=) p.(=)