CLC Genomics workbench and dbSNP VCF import

Question

[むらい]

I have tried to import a dbSNV vcf file into my workbench's reference genome, but error like that occurred and i am now, not able to make dbSNV track. The error :

Time    Elapsed time    Description
Sat Aug 10 21:21:47 GMT+09:00 2024  0:00:00 Skipped line 7 of C:\Users\myname\OneDrive - affilication name \2024myfile\Dry\reference\intersection_10001.vcf: Input is not VCF format compliant: Missing required header line.

The VCF file I tried to import is like this:

##fileformat=VCFv4.1
##FILTER=<ID=q25,Description="Quality below 25">
##INFO=<ID=DP,Number=1,Type=Integer,Description="Total Depth">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read Depth">
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT SAMPLE1
1   135 .   C   T   28  PASS    DP=5    GT:GQ:DP    1|1:28:5
1   138 .   T   C   36  PASS    DP=5    GT:GQ:DP    1|1:36:5
1   346 .   C   T   32  PASS    DP=3    GT:GQ:DP    1|1:32:3

Could you please help me with solving this issue?

[GenoMax]

Since you are paying for a CLC license it may be easiest to work with their tech support. You can also share the data directly with them to see what is going wrong.