42784002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118395915-T-G

http://identifiers.org/hco/10/GRCh38#42784145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118395786-C-A

42784145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118395786-C-T

42784555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118395383-C-T

42784612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118395339-T-C

42784681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118395270-T-C

42784699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118395242-G-A

42784699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118395242-G-T

42785325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118394639-T-C

42785448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118394565-C-G

42785725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118394312-G-A

42785725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118394312-G-C

42786147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118394120-C-G

42787068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118393597-A-G

42787104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118393566-G-A

42787104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118393566-G-C

42787104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118393566-G-T

42787113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118393557-G-T

42790286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118390913-G-A

42790398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118390803-G-A

42790475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118390726-G-A

42790476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 118390725-C-T

42790548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118390654-A-G

42790570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118390628-G-A

42791400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118390354-C-G

42791660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118390147-C-T

http://identifiers.org/hco/10/GRCh38#42791861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118389941-C-A

42791861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118389941-C-T

http://identifiers.org/hco/10/GRCh38#42791862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118389940-C-A

42791862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118389940-C-T

42792243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118389376-G-A

42792257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118389358-G-A

http://identifiers.org/hco/10/GRCh38#42792284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118389331-A-C

42792330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118389281-T-A

42792342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118389269-G-A

42792342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118389269-G-T

42792352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118389264-T-G

42792356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118389260-G-A

42792379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118389237-A-G

42792379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118389237-A-T

http://identifiers.org/hco/10/GRCh38#42792408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118389208-A-C

42792408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118389208-A-G

42792443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118389087-A-G

42792444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118389086-T-A

42792444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118389086-T-C

42792575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118388953-G-A

42792575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118388953-G-C

42792674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118388872-T-C

42792836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118388755-G-A

42792836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118388755-G-T

42792871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118388722-T-C

42792898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118388698-A-G

42792909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118388687-T-G

http://identifiers.org/hco/10/GRCh38#42793013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118388578-C-A

42793013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118388578-C-G

42793022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 118388569-C-T

42793061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118388530-T-A

http://identifiers.org/hco/10/GRCh38#42793191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118388409-C-A

42793192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118388408-T-C

42793222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118388385-G-A

42793222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118388385-G-T

http://identifiers.org/hco/10/GRCh38#42793343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118388280-C-A

42793369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118388252-T-C

42793385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118388236-A-T

42793408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118388212-C-T

42793739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118385433-A-G

42793745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118385427-G-T

42793762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118385404-C-G

42793897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118385064-A-G

42793993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 118384968-T-C

42794019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118384942-T-G

42794026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118384917-A-G

42794026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118384917-A-T

http://identifiers.org/hco/10/GRCh38#42794109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118384666-C-A

42794444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118384306-G-C

42794444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118384306-G-T

42794462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118384289-C-T

42794572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118384201-A-G

42796320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118382643-A-G

42796320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118382643-A-T

http://identifiers.org/hco/10/GRCh38#42796380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118382376-C-A

42796380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118382376-C-T

42796410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118382354-G-A

42796410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118382354-G-T

42796426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118382346-C-T

42796688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118382073-G-A

http://identifiers.org/hco/10/GRCh38#42796703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118382058-A-C

42796754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118382004-A-G

42796760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118381998-G-A

42796783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118381975-G-A

42796783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118381975-G-C

42796784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118381974-G-A

42796784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118381974-G-C

42796896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118381865-T-A

42796922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118381839-C-T

42796946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118381815-C-G

42797046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118381718-G-T

42797063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118381701-T-C

42797074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118381690-A-G

42797102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118381665-C-T

42797104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118381663-T-G

http://identifiers.org/hco/10/GRCh38#42797117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118381653-A-C

42797132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118381638-G-T

42797146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118381624-C-G

42797146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118381624-C-T

42797256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118381490-T-C

42797324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118381424-G-T

42797347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118381391-T-C

http://identifiers.org/hco/10/GRCh38#42797636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118380939-C-A

42797662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118380842-T-A

42797662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118380842-T-C

42798116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118380516-G-A

42798233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118380413-C-T

42798243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118380403-G-A

42798331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118380329-G-T

http://identifiers.org/hco/10/GRCh38#42798345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118380316-C-A

42798345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118380316-C-G

42798345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118380316-C-T

http://identifiers.org/hco/10/GRCh38#42798349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118380312-C-A

42798349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118380312-C-G

42798373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118380287-G-C

42798373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118380287-G-T

http://identifiers.org/hco/10/GRCh38#42798386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118380274-C-A

42798386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118380274-C-G

42798386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118380274-C-T

http://identifiers.org/hco/10/GRCh38#42798584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118380089-A-C

42798605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118380068-C-T

42798614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118380059-G-A

42798720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118379857-T-C

42798859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118379726-C-G

42798859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118379726-C-T

42801409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118375787-A-G

42801432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118375765-A-G

42801520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118375674-C-G

http://identifiers.org/hco/10/GRCh38#42801563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118375632-A-C

42801710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118375482-A-G

42801710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118375482-A-T

http://identifiers.org/hco/10/GRCh38#42802070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118375172-C-A

http://identifiers.org/hco/10/GRCh38#42802090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118375160-C-A

42802090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118375160-C-T

42802222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118375029-A-T

42815533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118374516-T-C

42815551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118374498-T-C

42815555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118374494-C-T

http://identifiers.org/hco/10/GRCh38#42815661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118374373-C-A

42815674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118374360-T-C

42815684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118374350-T-G

42815687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118374347-G-A

42816465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373901-G-A

42816465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373901-G-C

42816465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373901-G-T

http://identifiers.org/hco/10/GRCh38#42816518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118373859-C-A

42816518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373859-C-T

http://identifiers.org/hco/10/GRCh38#42816589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118373804-C-A

http://identifiers.org/hco/10/GRCh38#42816769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118373631-C-A

42816769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373631-C-T

42816786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373618-T-C

42816786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373618-T-G

42816787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373617-T-G

42816876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373577-C-T

42816952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373530-G-A

42816983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373514-T-C

42817091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373424-C-T

42817273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373306-G-A

42817273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373306-G-C

42817273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373306-G-T

http://identifiers.org/hco/10/GRCh38#42817512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118373071-C-A

42817512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373071-C-G

42817512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118373071-C-T

http://identifiers.org/hco/10/GRCh38#42820091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118370074-C-A

42820091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118370074-C-T

42820142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118370025-T-G

42820443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118369742-T-A

42820676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 118369515-G-A

42820725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118369477-A-G

42820726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118369476-T-C

42820727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118369475-T-A

42820820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118369387-G-C

42820984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense variant
orthologous variants: 118369285-G-T

42821068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118369208-G-T

http://identifiers.org/hco/10/GRCh38#42821105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118369170-A-C

42821267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118368850-A-G

42821333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118368755-A-G

42821406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118368684-G-C

42821454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118368636-T-C

42821510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118368590-T-C

42822005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118368292-T-C

42822051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118368250-G-A

42822051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118368250-G-C

42822051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118368250-G-T

42822052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118368249-T-C

http://identifiers.org/hco/10/GRCh38#42822204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118368097-C-A

42822204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118368097-C-T

42822212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118368092-T-C

42822212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118368092-T-G

42822831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118366569-G-T

http://identifiers.org/hco/10/GRCh38#42823040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118366390-A-C

42823040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118366390-A-G

42823040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118366390-A-T

http://identifiers.org/hco/10/GRCh38#42823102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118366359-C-A

42823190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, missense_variant
orthologous variants: 118366273-G-A

42823212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, missense_variant
orthologous variants: 118366251-G-A

42823212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron_variant, missense_variant
orthologous variants: 118366251-G-C

http://identifiers.org/hco/10/GRCh38#42823391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118366088-C-A

42823391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118366088-C-G

42823504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118365967-A-G

42823668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense_variant, undefined
orthologous variants: 118365831-A-G

http://identifiers.org/hco/10/GRCh38#42823795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118365704-C-A

42823795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118365704-C-T

42823817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118365682-G-A

42823817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118365682-G-T

42824028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118365457-A-G

42824252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118365272-T-C

42829946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118361682-A-G

42830134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118361498-G-T

42830142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118361490-A-T

http://identifiers.org/hco/10/GRCh38#42830145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118361487-C-A

42830145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118361487-C-T

42830232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118361393-T-G

42830247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118361379-G-A

42830565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118361114-T-C

42830602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118361084-T-A

42830683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118361012-T-C

42830725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118360970-C-G

42830771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118360939-T-C

42830771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: intron variant
orthologous variants: 118360939-T-G

42831061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense variant
orthologous variants: 118360639-T-A

42831081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: synonymous variant
orthologous variants: 118360619-G-A

42831081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense variant
orthologous variants: 118360619-G-T

42831083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense variant
orthologous variants: 118360617-G-A

42831083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: missense variant
orthologous variants: 118360617-G-T

42831159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360571-T-C

42831159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360571-T-G

http://identifiers.org/hco/10/GRCh38#42831179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118360555-A-C

42831179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360555-A-T

42831257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360478-T-G

42831284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360452-G-A

42831284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360452-G-T

42831292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360443-G-A

42831292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360443-G-T

42831413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360330-A-G

42831413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360330-A-T

42831428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360316-G-A

42831428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360316-G-T

42831433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360311-A-G

http://identifiers.org/hco/10/GRCh38#42831458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118360285-A-C

http://identifiers.org/hco/10/GRCh38#42831468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118360275-C-A

42831476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360267-T-A

42831476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360267-T-C

42831503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23505
most severe consequence: 3 prime UTR variant
orthologous variants: 118360246-G-A