109748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: 103367824-C-T

109901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: 103368045-T-G

109970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: 103368130-G-C

http://identifiers.org/hco/3/GRCh38#110011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103368172-C-A

110208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: 103368606-T-C

110215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: 103368613-T-C

110256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: 103368644-G-A

110292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: 103368675-C-T

110663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: 103369041-T-C

110800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: 103369170-A-G

110993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: 103369362-G-T

111244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: 103369608-A-T

111249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: 103369613-G-A

http://identifiers.org/hco/3/GRCh38#111443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103369803-C-A

111456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: 103369818-A-T

111543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: 103369904-C-T

114904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103372069-G-C

115014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103372169-A-G

115037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103372231-C-G

115037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103372231-C-T

115336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103372535-G-A

115762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103372985-T-C

115773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103372996-T-A

115779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103373002-T-C

115782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103373005-T-C

115819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103373044-G-C

115830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103373049-T-G

115879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: non coding transcript exon variant
orthologous variants: 103373099-T-C

116230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103373465-A-G

116335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103373567-G-A

116335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103373567-G-T

116380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103373612-G-C

116824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103374234-G-A

116981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103374386-G-T

116998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103374403-C-T

116999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103374404-T-C

117119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103374525-A-T

http://identifiers.org/hco/3/GRCh38#117134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103374543-A-C

117450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103374867-C-T

117459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103374876-A-G

http://identifiers.org/hco/3/GRCh38#117597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103374987-C-A

117600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103374990-T-C

117600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103374990-T-G

http://identifiers.org/hco/3/GRCh38#117687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103375057-C-A

117777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103375171-G-A

117851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103375231-C-T

http://identifiers.org/hco/3/GRCh38#120784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103379179-A-C

120784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379179-A-T

120847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379237-G-A

121144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379745-A-G

http://identifiers.org/hco/3/GRCh38#121204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103379804-C-A

121336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379936-T-C

121367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379966-T-C

121368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379967-A-G

121377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379976-T-C

121398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103379997-G-T

http://identifiers.org/hco/3/GRCh38#121479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103380087-C-A

121646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103380253-A-T

121800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103380414-A-G

121800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103380414-A-T

121890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103380517-G-C

122002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103380714-A-G

http://identifiers.org/hco/3/GRCh38#122011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103380737-C-A

122011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103380737-C-G

122070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103380789-A-G

122157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103380873-T-A

122373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381056-G-C

122398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381088-A-G

122449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381192-T-C

122449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381192-T-G

122470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381210-C-T

122533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381271-T-C

122624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381359-A-G

122662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381414-T-G

122880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381813-T-A

122976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381905-G-A

123028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103381955-G-A

123232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382140-A-G

123245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382153-G-T

http://identifiers.org/hco/3/GRCh38#123280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103382188-A-C

123293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382201-A-G

123301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382209-T-C

123493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382397-A-G

123504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382409-A-T

124604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382548-G-C

124657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382598-G-A

124770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382716-C-T

124811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382751-A-G

124829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103382769-G-T

128095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103394967-A-T

128137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103394996-T-G

128184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103395048-T-C

128272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103395136-T-C

128322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103395187-G-A

http://identifiers.org/hco/3/GRCh38#128498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103395327-C-A

128594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103395421-G-A

128762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103395585-G-A

128847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103395675-C-T

129066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103395889-C-T

129139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103395951-G-C

129232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103396060-G-A

129246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103396072-C-T

http://identifiers.org/hco/3/GRCh38#129343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103396165-C-A

129343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103396165-C-T

http://identifiers.org/hco/3/GRCh38#129515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103396219-A-C

129576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103396279-T-C

129605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 103396303-G-A

129605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 103396303-G-C

129657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103396355-C-G

129680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103396378-G-C

129708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103396407-G-A

129708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103396407-G-C

129732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103396430-C-G

129732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103396430-C-T

129770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103396468-G-C

129822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103396503-T-C

130180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103396611-G-C

130377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103396870-C-T

130518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397076-G-A

130579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397126-C-T

130580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397127-A-G

http://identifiers.org/hco/3/GRCh38#130632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103397172-C-A

130700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397214-A-G

130851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397389-T-G

http://identifiers.org/hco/3/GRCh38#130880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103397418-A-C

130880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397418-A-G

130880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397418-A-T

131026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397510-G-A

131165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397650-C-T

131274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397758-T-A

131285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397770-C-T

131290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397775-T-C

131292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397777-G-C

131305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397782-C-G

131324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397800-C-G

131325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397801-C-G

131403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397879-T-C

131467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103397918-A-G

131601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103398058-C-T

131961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103398419-G-A

131961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103398419-G-C

http://identifiers.org/hco/3/GRCh38#132275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103398726-C-A

132275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103398726-C-G

132275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103398726-C-T

132287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103398738-T-C

http://identifiers.org/hco/3/GRCh38#132449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103399026-C-A

132644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103399302-T-C

133005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103399603-A-G

133235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103399766-T-C

136166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103401703-T-G

http://identifiers.org/hco/3/GRCh38#136375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103401893-A-C

136406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103401912-A-G

http://identifiers.org/hco/3/GRCh38#136689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103402178-C-A

136696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402185-A-G

136975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402503-T-C

137046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402573-A-G

http://identifiers.org/hco/3/GRCh38#137125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103402649-C-A

137125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402649-C-G

137246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103402772-G-A

137740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103403243-A-G

139884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103406029-T-C

http://identifiers.org/hco/3/GRCh38#139957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103406094-C-A

139965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103406098-A-G

140241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103407330-A-G

140257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103407345-G-C

140537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103407621-A-G

140620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103407702-T-C

140666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103407749-A-T

140728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103407810-T-A

140728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103407810-T-C

140833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103407913-A-T

http://identifiers.org/hco/3/GRCh38#141012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103408093-A-C

http://identifiers.org/hco/3/GRCh38#141014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103408095-A-C

141014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103408095-A-G

141026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103408107-G-C

141078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103408160-C-T

141118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103408200-G-A

141118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103408200-G-C

141137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103408219-C-T

http://identifiers.org/hco/3/GRCh38#141653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103408722-A-C

141716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103408772-T-G

http://identifiers.org/hco/3/GRCh38#146036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103411856-C-A

146036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103411856-C-G

146086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103411908-C-T

146602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103416907-C-T

146663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103416983-T-A

146703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103417023-A-T

146860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103417175-C-T

http://identifiers.org/hco/3/GRCh38#146874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103417189-C-A

146887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103417200-G-C

146887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103417200-G-T

146980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103417290-T-C

147066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103417375-T-C

147097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103417389-C-T

http://identifiers.org/hco/3/GRCh38#147133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103417419-C-A

147133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103417419-C-T

147139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103417425-G-A

147206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103417533-C-G

147236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103417633-A-G

147448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103417835-C-T

147469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103417856-G-C

147485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103417874-T-G

147776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103418192-C-G

147824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103418236-A-G

147981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103418359-G-C

148048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103418426-C-G

148048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103418426-C-T

148277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103418651-T-C

148345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103418719-G-A

148345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103418719-G-C

148553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103418921-G-A

149026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103419419-C-G

149064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103419452-G-A

149065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103419453-G-A

149065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103419453-G-C

149117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103419521-A-G

http://identifiers.org/hco/3/GRCh38#149203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103419611-C-A

149247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103419838-C-T

149359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103419951-G-A

149540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103420583-C-G

http://identifiers.org/hco/3/GRCh38#149759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103420831-C-A

149829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103420903-G-C

150763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103421790-A-G

150767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103421794-C-T

150875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103421899-G-A

150875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103421899-G-C

150886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103421910-A-G

150996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103422016-G-C

152604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103427579-A-T

http://identifiers.org/hco/3/GRCh38#152694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103427664-A-C

153048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103427989-C-T

153063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103428003-A-G

153080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103428020-A-G

153192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103428124-G-A

153192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103428124-G-T

153212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103428138-G-A

153745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103428677-G-A

153745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103428677-G-T

153842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103428774-A-T

153863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103428795-G-A

153881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103428812-T-C

153942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103428861-C-T

153950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103428869-G-A

155823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103434836-C-T

155862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103434875-C-G

155876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103434889-G-T

http://identifiers.org/hco/3/GRCh38#155924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103434937-C-A

156138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103435126-G-A

156410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103435394-T-C

156412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103435396-G-A

156412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103435396-G-C

156600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103435588-G-A

156627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103435615-T-C

156700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103435679-G-C

156741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103435716-C-T

http://identifiers.org/hco/3/GRCh38#157661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103435963-C-A

157661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103435963-C-T

158044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103436334-G-A

158276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103437280-C-T

158471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103437475-C-T

158473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103437477-G-A

158634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103437641-C-T

158750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103437759-G-T

159193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103438792-C-T

159329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103438931-A-T

159566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103439157-A-G

159711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103439305-C-T

159832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103439425-T-G

159943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103439528-T-C

159974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103439559-A-G

160044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103439627-A-G

160211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103439800-G-T

160277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103439866-T-G

160358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103439937-C-T

http://identifiers.org/hco/3/GRCh38#160570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103440150-C-A

160570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103440150-C-G

http://identifiers.org/hco/3/GRCh38#165169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103448631-A-C

165190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103448652-G-A

165358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103448839-A-T

165570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103449042-G-A

165570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103449042-G-C

165570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103449042-G-T

165665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103449132-A-G

165974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103449438-T-G

165992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103449456-T-C

166037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103449470-G-A

166126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103449546-A-G

166539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103449975-T-C

166547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103449981-T-C

166695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103450111-A-T

166876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103450290-G-A

166999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103450411-C-T

167019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103450430-G-A

167316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103450719-C-T

167644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103451067-C-T

167745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103451154-C-G

168258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103451716-T-C

168410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103451868-G-A

168410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103451868-G-C

168540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103451982-G-T

168643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103452083-T-C

168695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103452115-A-G

168695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103452115-A-T

168710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103452130-G-A

168720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103452137-A-G

169710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103452271-C-G

http://identifiers.org/hco/3/GRCh38#169763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103452322-C-A

169986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103452549-A-G

http://identifiers.org/hco/3/GRCh38#170568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103453047-C-A

170814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103453511-C-T

170946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103453696-C-T

172537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103463227-A-G

172593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103463283-A-G

172822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103463511-G-T

172926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103463617-C-G

173131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103463749-C-T

173135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103463754-A-T

173331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103463870-A-T

http://identifiers.org/hco/3/GRCh38#173536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103463912-C-A

173536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103463912-C-T

173896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103464171-T-C

174208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103464509-G-T

174410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103464712-C-G

174625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103465061-G-A

174783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103465222-T-A

174842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103465283-G-A

174842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103465283-G-C

175173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103465629-C-T

http://identifiers.org/hco/3/GRCh38#175222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103465682-A-C

175350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103465799-T-C

175450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103465898-G-A

175492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103465935-T-C

175656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466109-G-T

175813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466296-G-A

175835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466321-T-C

175892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466393-G-T

175968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466447-G-C

176098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466584-C-T

176139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466627-A-G

176247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466722-G-C

176967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466840-G-A

176981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466854-G-A

177029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466891-T-C

177071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466929-G-T

177091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466947-G-A

http://identifiers.org/hco/3/GRCh38#177107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103466963-C-A

177140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103466996-A-G

177157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103467011-G-A

177180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103467023-T-G

177228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103467074-A-G

177251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103467097-G-C

177266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103467112-T-G

177317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103467163-A-G

177330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103467176-G-A

177361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103467205-T-C

http://identifiers.org/hco/3/GRCh38#177408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103467242-A-C

178100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103467997-A-G

http://identifiers.org/hco/3/GRCh38#178108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103468006-C-A

178113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468011-C-T

178148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468050-T-C

178163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468065-G-A

178163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468065-G-C

178175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468075-T-C

178175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468075-T-G

178184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468084-G-A

178214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468133-T-A

178220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468139-G-C

178226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468145-G-A

178255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468176-G-A

178255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468176-G-C

178399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468239-T-G

178451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468301-G-A

178480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468320-T-A

178499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468337-G-C

178527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468369-G-A

178573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468414-T-G

178781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468619-T-C

178842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468677-G-T

178848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468683-A-G

178848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468683-A-T

178950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468784-A-G

178962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468796-T-C

178963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468798-C-T

http://identifiers.org/hco/3/GRCh38#178998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103468835-C-A

179001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103468842-C-T

179477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103469752-G-A

181291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103470351-A-G

182561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103471973-T-C

182970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103472062-A-T

183008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103472095-T-A

183113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103472188-A-T

http://identifiers.org/hco/3/GRCh38#183234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103472306-A-C

183304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103472378-A-G

183488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103473998-G-T

183735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474238-T-C

183806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474275-C-T

183878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474346-G-A

184030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474502-C-T

184080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474551-A-G

184162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474631-A-G

184227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474695-G-A

184227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474695-G-T

184328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474786-G-T

184538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103474983-A-G

184673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103475127-C-T

184730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103475188-A-G

184764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103475223-T-A

184962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103475419-C-T

184971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103475428-T-C

185055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103475513-C-T

185143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103475601-T-C

http://identifiers.org/hco/3/GRCh38#185215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103475672-C-A

185216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103475673-G-A

185216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103475673-G-C

185933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103476583-G-T

186098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103476725-G-A

186098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103476725-G-C

186228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103476852-G-A

186410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103477047-A-G

186465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103477105-A-G

186470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103477110-G-A

186568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103477216-G-A

186612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103477255-T-C

186789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103477408-T-G

186868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103477482-A-G

186946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103477561-G-C

186946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103477561-G-T

191072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103477994-G-T

191122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103478058-A-G

191159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103478094-T-C

191677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103482422-T-A

191747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103482492-G-C

191772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103482517-T-C

191815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103482558-A-G

http://identifiers.org/hco/3/GRCh38#193534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103484330-A-C

193534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103484330-A-G

http://identifiers.org/hco/3/GRCh38#193826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103484612-C-A

194041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103484802-G-A

194041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103484802-G-C

194106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103484867-A-G

194472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103485227-A-G

194493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103485248-A-G

194779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103485481-G-A

194779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103485481-G-C

194852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103485557-C-T

194910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103485725-T-C

194960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103485794-C-T

195103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103485980-C-G

195131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103486008-C-T

195188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103486067-G-A

195188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103486067-G-T

195211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103486090-C-T

195367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103486410-T-C

195621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103486654-A-G

195644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103486677-C-T

http://identifiers.org/hco/3/GRCh38#195699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103486732-C-A

195961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103486962-G-A

196023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103487024-A-T

196082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103487092-T-C

196201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103487217-C-T

196329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103487349-G-T

196450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103487472-A-G

196456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103487494-A-G

http://identifiers.org/hco/3/GRCh38#196497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103487533-C-A

196497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103487533-C-T

http://identifiers.org/hco/3/GRCh38#196505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103487541-C-A

196505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103487541-C-T

196569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103487606-A-G

196569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103487606-A-T

196586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103487625-A-G

196586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103487625-A-T

196593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103487632-A-G

196593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103487632-A-T

196601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103487640-T-C

http://identifiers.org/hco/3/GRCh38#196606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103487645-C-A

196606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 103487645-C-G

196606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 103487645-C-T

196619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103487661-G-T

http://identifiers.org/hco/3/GRCh38#196723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103487766-A-C

196742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103487785-G-A

http://identifiers.org/hco/3/GRCh38#196802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#103487850-C-A

196802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103487850-C-T

196814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103487862-G-A

196814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103487862-G-T

http://identifiers.org/hco/3/GRCh38#196819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#103487867-C-A

196819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103487867-C-G

196819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103487867-C-T

196877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103487923-G-A

196877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103487923-G-T

196907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103487953-C-G

197074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103488140-G-A

197074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103488140-G-T

http://identifiers.org/hco/3/GRCh38#197086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103488153-C-A

197086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103488153-C-T

http://identifiers.org/hco/3/GRCh38#197121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#103488184-C-A

197121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103488184-C-T

197142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103488206-G-A

197142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103488206-G-C

197142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103488206-G-T

197185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103488251-G-T

197192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103488259-G-T

197210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103488281-G-A

197210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103488281-G-T

197249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103488319-G-A

197249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103488319-G-C

197258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103488328-T-C

197258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103488328-T-G

http://identifiers.org/hco/3/GRCh38#197318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#103488390-C-A

197318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103488390-C-G

197318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40147
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103488390-C-T