74316223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84856087-C-G

74316223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84856087-C-T

74316318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84856005-G-A

74317022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron_variant, undefined
orthologous variants: 84855843-T-C

74317154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84855717-G-C

74317205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84855666-C-G

74317205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84855666-C-T

74317229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84855642-T-C

74317430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84855449-T-C

74317528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84855169-C-T

74317686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84855020-G-T

74317698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84855008-T-C

74317698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84855008-T-G

http://identifiers.org/hco/18/GRCh38#74317699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84855006-A-C

74317699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84855006-A-T

74317775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84854932-G-A

74317775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84854932-G-C

74317775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84854932-G-T

74317787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84854920-T-C

74317795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84854912-A-G

74317887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84854818-T-C

74317887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84854818-T-G

74317902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84854803-A-G

74317949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84854756-T-G

74318002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84854703-A-G

74318037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84854669-T-C

74318038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84854668-T-C

74318061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84854643-A-G

74318105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84854608-G-T

http://identifiers.org/hco/18/GRCh38#74318298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84854236-A-C

74318298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84854236-A-T

74318314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84854220-T-G

74318368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84854191-G-A

http://identifiers.org/hco/18/GRCh38#74319090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84853739-C-A

74320583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84853500-G-A

74320583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84853500-G-T

74320744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84853369-A-G

74320793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84853324-A-T

74320855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84853262-G-T

74320890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84853226-T-C

74322421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84852377-G-A

74322510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84852292-G-C

74322565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84852228-A-G

74322583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84852204-G-A

74322583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84852204-G-T

74322590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84852197-G-A

74322590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84852197-G-T

http://identifiers.org/hco/18/GRCh38#74322637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84852128-C-A

74322637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84852128-C-T

74322706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: synonymous variant
orthologous variants: 84851877-T-C

74322776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84851805-T-A

74322776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84851805-T-C

74322786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84851793-T-A

74322786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84851793-T-C

74322839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84848565-G-T

http://identifiers.org/hco/18/GRCh38#74322871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84848533-A-C

74322871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84848533-A-G

74322897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84848510-A-G

74327590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84844188-T-C

74327745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84844056-T-C

74327804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84843998-A-G

http://identifiers.org/hco/18/GRCh38#74327837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84843965-C-A

74327837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84843965-C-T

74328075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84843733-A-G

74328081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84843727-T-C

74328082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84843726-G-A

74328121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84843702-T-C

74328673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84843327-G-A

74328709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84843284-G-C

http://identifiers.org/hco/18/GRCh38#74328715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84843278-C-A

74328715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84843278-C-G

74328835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84843158-T-C

http://identifiers.org/hco/18/GRCh38#74328921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84843090-A-C

74328970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84843043-T-C

74328970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84843043-T-G

http://identifiers.org/hco/18/GRCh38#74328979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84843034-C-A

74328979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84843034-C-T

74328996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 84843017-A-G

74329016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84842997-T-A

74329016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84842997-T-C

74329074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84842936-T-A

74329074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84842936-T-C

74329842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84842432-G-T

74330245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84842045-T-G

http://identifiers.org/hco/18/GRCh38#74330269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84842019-C-A

74330270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84842018-A-G

74330726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84841725-A-G

74330731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84841720-A-T

74330803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84841674-A-G

74330823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84841655-G-A

74330823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84841655-G-T

74330828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84841650-A-G

74330840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84841638-T-C

http://identifiers.org/hco/18/GRCh38#74330842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84841636-C-A

74330842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84841636-C-T

74330843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84841635-A-G

74330843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84841635-A-T

74330909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84841573-A-G

74330913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84841569-G-A

74330913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84841569-G-C

http://identifiers.org/hco/18/GRCh38#74330928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84841554-C-A

74330928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84841554-C-G

74330928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: synonymous variant
orthologous variants: 84841554-C-T

http://identifiers.org/hco/18/GRCh38#74330935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84841547-C-A

74330935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84841547-C-G

74330935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84841547-C-T

74330986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84841497-T-A

74330986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84841497-T-C

74330994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84841489-A-G

74331005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84841480-T-C

74331005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84841480-T-G

74331253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84840816-T-G

74331309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84840765-C-T

74331522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84840572-T-C

74331522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84840572-T-G

74331555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84840539-G-T

http://identifiers.org/hco/18/GRCh38#74331602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#84840473-A-C

74331602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron_variant, undefined
orthologous variants: 84840473-A-G

74331668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84840419-T-A

74331673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84840414-C-T

74334764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84840073-A-G

74335025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84839813-T-A

74335081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84839773-C-G

http://identifiers.org/hco/18/GRCh38#74335149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84839704-A-C

http://identifiers.org/hco/18/GRCh38#74335189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84839666-A-C

74335216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84839643-T-A

74335587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84839342-C-T

74336748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84836735-G-C

74336779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84836707-C-G

74336830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84836648-C-T

74337007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84836502-T-A

74337342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84836221-A-G

http://identifiers.org/hco/18/GRCh38#74337350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84836216-A-C

http://identifiers.org/hco/18/GRCh38#74338427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84835492-A-C

74338592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84835334-T-C

74338595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84835330-C-T

74338651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84835288-T-A

74338651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84835288-T-C

74339289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84834167-A-G

74339341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84834133-T-C

74339369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84834110-A-G

74339459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84834036-A-G

74339742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84833763-C-T

74339749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84833756-G-A

http://identifiers.org/hco/18/GRCh38#74342012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84828310-C-A

http://identifiers.org/hco/18/GRCh38#74342071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84828252-C-A

http://identifiers.org/hco/18/GRCh38#74342073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84828250-C-A

74342073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84828250-C-T

74342168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84828157-A-G

74342175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84828151-T-C

74342263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84828063-A-G

74342263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84828063-A-T

http://identifiers.org/hco/18/GRCh38#74342357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84827969-C-A

74342357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84827969-C-T

74342398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84827914-T-A

74342398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84827914-T-C

74342461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84827728-T-A

74342659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84827266-T-C

74342937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84827107-T-C

http://identifiers.org/hco/18/GRCh38#74343243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84826820-C-A

74343243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84826820-C-T

74343307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84826742-T-C

74343336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84826703-A-G

74343435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84826632-G-T

74343495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84826582-A-G

74343533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84826544-G-C

74343721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84826356-T-C

74343751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84826331-T-A

74343889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84826221-A-G

74343956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84826163-G-A

74344027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84826105-A-G

74344027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84826105-A-T

74344148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84826006-T-C

74344162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84825992-T-C

74346531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84822244-C-T

74347977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84821890-T-C

74347983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84821884-A-G

74348140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84821730-C-T

74348179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84821690-G-T

74348343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84821545-G-A

http://identifiers.org/hco/18/GRCh38#74348626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84820986-A-C

74348686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84820933-A-G

74348764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84820338-A-G

74348764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84820338-A-T

74348971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84820138-G-T

http://identifiers.org/hco/18/GRCh38#74349045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84820082-C-A

74349045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84820082-C-G

74349091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84820027-T-G

74349119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84819999-C-G

74349131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84819987-C-T

74349364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84819752-G-A

74349387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84819730-C-G

74349401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84819715-T-C

http://identifiers.org/hco/18/GRCh38#74350268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84819257-A-C

74350269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84819256-G-T

74350330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84819215-C-T

74352559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84818338-A-T

74352756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84818149-G-A

74352768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84818137-A-G

74352820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84818110-T-C

74352991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84817971-T-A

74353104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84817909-T-G

74353122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84817894-A-G

74353167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84817852-G-T

74353170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84817849-A-T

74353203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84817815-T-C

74353218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84817800-A-T

74353290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: synonymous variant
orthologous variants: 84817731-T-C

74353291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84817730-A-G

74353312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84817709-A-G

74353444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84817577-C-G

74353444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: stop gained
orthologous variants: 84817577-C-T

74353485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: synonymous variant
orthologous variants: 84817536-A-G

http://identifiers.org/hco/18/GRCh38#74353515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84817506-A-C

74353649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84817372-A-G

74353669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: synonymous variant
orthologous variants: 84817352-T-C

http://identifiers.org/hco/18/GRCh38#74353677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84817344-A-C

74353903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84817130-G-C

74353981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84817052-T-G

74354026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84817007-T-A

74354026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84817007-T-G

74354126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84816907-T-C

74354144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84816889-G-T

74354230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84816803-A-T

74354263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: stop gained
orthologous variants: 84816773-A-T

http://identifiers.org/hco/18/GRCh38#74354276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84816760-A-C

74354288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84816756-G-A

74354288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84816756-G-C

74354289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84816755-G-C

74354289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84816755-G-T

74354298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84816746-A-G

74354298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84816746-A-T

http://identifiers.org/hco/18/GRCh38#74354321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84816724-C-A

74354321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84816724-C-T

74354436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84815851-T-G

74354466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84815827-T-A

74354466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: missense variant
orthologous variants: 84815827-T-C

74354483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: synonymous variant
orthologous variants: 84815810-T-C

74354521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84815776-A-G

74354558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84815747-G-A

74354561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84815744-A-G

74354798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84815557-C-G

74354838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84815515-A-G

74354878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84815473-A-T

74354996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84815363-G-C

74355109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: intron variant
orthologous variants: 84815251-C-T

74356505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84814463-G-T

74356557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84814410-C-T

74356598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84814368-T-C

74356637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84814328-G-A

74356637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84814328-G-T

74356646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84814319-T-C

74356677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84814287-C-T

http://identifiers.org/hco/18/GRCh38#74356762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84814042-A-C

74356762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84814042-A-G

74356920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84813836-A-T

74356957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84813799-C-T

74356975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84813779-T-C

74357052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84813676-C-T

74357056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84813606-A-G

http://identifiers.org/hco/18/GRCh38#74357068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84813594-C-A

74357170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84813453-T-C

74357193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84813430-A-G

74357195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84813428-T-C

74357236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84813399-G-A

74357236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84813399-G-T

74357269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84813371-G-A

74357269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84813371-G-C

74357270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84813370-C-T

74357378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84813291-T-A

http://identifiers.org/hco/18/GRCh38#74357652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84812938-A-C

74357963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84812658-C-T

74357970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84812651-G-C

74357970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84812651-G-T

http://identifiers.org/hco/18/GRCh38#74357976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84812645-C-A

http://identifiers.org/hco/18/GRCh38#74358279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84812050-C-A

74358293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84812037-T-C

http://identifiers.org/hco/18/GRCh38#74358393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84811896-A-C

74358457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84811839-G-A

74358476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84811820-A-G

74358644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84811417-T-C

74358696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84811374-T-G

74358798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84811269-G-T

http://identifiers.org/hco/18/GRCh38#74358860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#84811221-A-C

74359001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84811084-G-T

74359038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84811048-T-C

74359065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40037
most severe consequence: 3 prime UTR variant
orthologous variants: 84811021-G-T