feat: Add clinvarID to VCF (#1547)

#### Changed

- renamed CLNACC to CLNVID for Clinvar annotations

Author: mathiasbio

BALSAMIC/workflows/balsamic.smk

@@ -188,7 +188,7 @@ research_annotations.append(
             {
                 "file": Path(config["reference"]["clinvar"]).as_posix(),
                 "fields": [
-                    "CLNACC",
+                    "CLNVID",
                     "CLNREVSTAT",
                     "CLNSIG",
                     "ORIGIN",
@@ -202,7 +202,7 @@ research_annotations.append(
                 ],
                 "ops": ["self", "self", "self", "self", "self", "self", "self", "self", "self", "self", "self"],
                 "names": [
-                    "CLNACC",
+                    "CLNVID",
                     "CLNREVSTAT",
                     "CLNSIG",
                     "ORIGIN",

CHANGELOG.rst

@@ -26,6 +26,7 @@ Changed:
 * Updated cluster resources for tnscope WGS TN https://github.com/Clinical-Genomics/BALSAMIC/pull/1535
 * Disable SV calling in TNscope https://github.com/Clinical-Genomics/BALSAMIC/pull/1541
 * Remove VarDict parallelization per chromosome https://github.com/Clinical-Genomics/BALSAMIC/pull/1544
+* Renamed CLNACC INFO field to CLNVID https://github.com/Clinical-Genomics/BALSAMIC/pull/1547
 
 Removed:
 ^^^^^^^^