Variant #0000995776 (NC_000006.11:g.43044661C>T, NC_000006.11(NM_002821.4):c.79+356C>T (PTK7))

Chromosome 6
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.43044661C>T
DNA change (hg38) -
Published as PTK7(NM_001270398.1):c.40C>T (p.(Pro14Ser))
ISCN -
DB-ID KLC4_000003
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) 9.0E-5 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 2024-08-28 13:16:32 +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     
PTK7 NM_002821.4 -?/. - c.79+356C>T r.(=) p.(=)
KLC4 NM_138343.2 -?/. - c.*9771C>T r.(=) p.(=)


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