121519106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117357142-A-G

http://identifiers.org/hco/1/GRCh38#121519107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117357143-A-C

121519107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117357143-A-G

121519112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117357148-A-G

121519186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117357228-G-A

121519186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117357228-G-C

121519215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117357257-T-C

121519215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117357257-T-G

121519288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117357331-G-A

121519288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117357331-G-T

121519296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117357339-G-A

121519296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117357339-G-C

121519296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117357339-G-T

http://identifiers.org/hco/1/GRCh38#121519399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117357433-C-A

121519399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117357433-C-G

121519399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117357433-C-T

http://identifiers.org/hco/1/GRCh38#121519472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117357508-C-A

121519472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117357508-C-T

121519498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117357535-G-A

121519498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117357535-G-T

121519590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117357627-G-A

121519590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117357627-G-T

121519597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357634-G-A

121519597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357634-G-T

121519598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357638-A-G

121519627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117357667-G-A

121519627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117357667-G-T

121519786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117357828-G-T

http://identifiers.org/hco/1/GRCh38#121519861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117357894-A-C

121519894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117357926-G-T

121520331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117358037-T-C

121520428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117358118-A-G

121520478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117358168-T-C

121520524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117358210-C-T

121520578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117358258-A-G

121520709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117358389-A-G

121520745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117358423-G-A

121521492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117358997-T-C

121521541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117359028-A-T

121521905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117359466-C-G

http://identifiers.org/hco/1/GRCh38#121522081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#117359674-C-A

121522081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117359674-C-T

http://identifiers.org/hco/1/GRCh38#121522293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#117359891-A-C

121522293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117359891-A-G

http://identifiers.org/hco/1/GRCh38#121522309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#117359909-C-A

121522685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360426-A-G

121523491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360601-C-T

http://identifiers.org/hco/1/GRCh38#121523492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117360602-C-A

121523545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360643-C-T

http://identifiers.org/hco/1/GRCh38#121523632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117360723-C-A

121523636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360727-C-T

121523679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360768-G-A

121523766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360834-G-A

121523821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360887-T-A

121523990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117361033-G-C

121524023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117361067-C-T

121524176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117361297-A-G

121524267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117361368-A-G

121524342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117361437-G-A

121524602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117361718-A-G

121524722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117361852-G-T

121525201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117362396-G-A

121525240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117362435-G-T

121525243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117362438-C-T

121525348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117362540-A-G

121525593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117363399-T-A

121526177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117364265-C-T

121526181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117364269-T-G

121527269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117364456-G-A

121527765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117364593-G-T

121528353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117366679-A-G

121528363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117366689-A-G

121528376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117366702-A-G

121528663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117366986-T-C

121528692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117367020-C-G

121528692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117367020-C-T

121528822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117367145-G-C

121528850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117367168-A-G

121528878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117367206-T-C

121528926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117367255-T-G

121529044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117367389-C-G

121529061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117367406-A-G

121529062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117367407-G-T

121529633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117368198-G-C

121529633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117368198-G-T

121529775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117368319-T-C

121529842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117368381-T-C

121529842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117368381-T-G

121539102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117369725-G-A

121539102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117369725-G-T

121539217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117369817-G-A

http://identifiers.org/hco/1/GRCh38#121539281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117369898-A-C

121539281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117369898-A-G

http://identifiers.org/hco/1/GRCh38#121539302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117369940-C-A

121539377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117370003-G-A

121539479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117370106-T-C

121539599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117370225-A-G

121539738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117370322-A-G

121539828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117370406-G-A

121539828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117370406-G-T

http://identifiers.org/hco/1/GRCh38#121539829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117370407-C-A

121539850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117370424-A-G

121539913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117370485-T-C

121539913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117370485-T-G

121541025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371015-A-G

http://identifiers.org/hco/1/GRCh38#121541036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117371026-C-A

121541082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371064-A-G

121541182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371180-G-A

121541193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371191-A-G

121541220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371221-G-T

121541296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371285-A-G

121541431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371460-G-T

121541438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371467-G-A

121541493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371521-G-A

121541502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371530-C-T

121541514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371533-T-C

121541607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371604-A-G

121542164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371856-T-G

121542177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371869-G-A

121542266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371928-T-A

121542266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371928-T-C

121542362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117372021-G-T

121542771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117372476-A-G

121542883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117372577-T-C

121542905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117372599-T-C

121542906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117372600-G-T

121550593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117377443-G-A

121550627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117377476-G-A

121550627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117377476-G-C

121551520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117378665-A-G

121551544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117378689-A-T

121551547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117378692-T-C

121551780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117378916-G-A

121551811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117378947-G-C

121551852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117378986-A-G

121551870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117379004-T-C

121551943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117379073-T-C

121552497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117380149-A-G

121552553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117380209-G-A

121552606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117380263-A-G

121552724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117380370-A-T

121552732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117380378-C-T

121552736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117380382-G-A

121552838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117380489-C-T

121552917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117380570-G-A

121552951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117380600-G-A

http://identifiers.org/hco/1/GRCh38#121556427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117385679-C-A

121556427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117385679-C-G

121556457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117385712-A-G

http://identifiers.org/hco/1/GRCh38#121556543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117385841-C-A

http://identifiers.org/hco/1/GRCh38#121556578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117385876-C-A

121556578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117385876-C-T

http://identifiers.org/hco/1/GRCh38#121556606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117385904-C-A

121556606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117385904-C-G

121556606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117385904-C-T

121556654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117385952-A-G

121556654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117385952-A-T

121556657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117385955-T-A

121556657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117385955-T-C

121556724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117386024-G-T

http://identifiers.org/hco/1/GRCh38#121556730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117386030-C-A

121556730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117386030-C-G

121556730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117386030-C-T

121556736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117386036-T-A

http://identifiers.org/hco/1/GRCh38#121556749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117386049-A-C

121556767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117386067-G-A

121556767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117386067-G-T

121556942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117386248-T-A

121557018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 117386321-A-G

121557018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 117386321-A-T

121557071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117386355-A-G

121557071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117386355-A-T

121557072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117386356-G-T

121557581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117392301-A-G

121557729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117392446-C-T

121557744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117392460-T-C

121558004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117392688-G-A

121558110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117392790-C-T

http://identifiers.org/hco/1/GRCh38#121558168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117392842-C-A

121558827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117394973-A-T

121558842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117394988-G-A

121558887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117395026-T-A

121558910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117395049-C-G

121558979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117395119-A-G

121559024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117395171-G-C

121559024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117395171-G-T

121559042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117395189-T-A

121559621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117395704-G-A

http://identifiers.org/hco/1/GRCh38#121559869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117396015-C-A

121559917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117396061-A-G

121559954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117396097-T-C

121559973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117396116-A-G

http://identifiers.org/hco/1/GRCh38#121560077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117396218-C-A

121560159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117396293-T-C

121561700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400357-T-G

121561710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400367-C-G

121561710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400367-C-T

121561846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400562-C-T

121561943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400638-C-G

http://identifiers.org/hco/1/GRCh38#121562103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117400805-A-C

http://identifiers.org/hco/1/GRCh38#121562162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117400864-C-A

121562162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400864-C-T

121562349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117401052-T-A

121562423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117401465-T-A

121562423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117401465-T-C

121562475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117401507-T-A

121562485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117401517-G-T

121562545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117401573-C-T

121562695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117402061-A-G

121562806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117402167-T-C

121562935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117402306-C-G

121562935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117402306-C-T

121563237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117402594-G-A

121563436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117402763-A-T

121563471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117402790-C-T

121563491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117402810-T-C

121563494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117402813-C-T

121563658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117402964-G-A

121563705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403010-A-G

121563734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403039-A-G

121563836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403152-G-T

121563887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403204-G-A

121563905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403222-G-A

121564021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403321-G-A

121564245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403479-T-A

121564375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403591-T-C

121564383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403599-T-A

121564385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403601-G-A

121564472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403688-C-T

121564491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403710-T-C

121564491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403710-T-G

121564510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403729-A-G

121564521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403740-G-A

121564521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403740-G-T

121564559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403774-T-C

121564584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403806-T-A

121564669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117403891-G-T

121564782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117404004-A-G

121564787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117404009-G-T

121564813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117404035-G-A

121564813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117404035-G-T

121564832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117404054-G-C

121564832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117404054-G-T

121564920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 117404142-T-C

121564938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117404163-T-G

121564991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117404184-T-C

121564993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117404186-G-T

121565038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117404230-A-G

121565523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405218-A-G

121565597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405316-T-C

121565613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405340-G-A

121565627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405354-T-A

121565701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405407-G-T

121565744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405441-A-T

121565750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405447-C-T

121565755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405457-G-C

121565817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405516-G-C

121565830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405528-T-C

http://identifiers.org/hco/1/GRCh38#121565842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117405539-C-A

121565842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405539-C-G

121565844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405541-G-A

121565942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405651-A-G

121566271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117406545-G-A

http://identifiers.org/hco/1/GRCh38#121566318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117406578-C-A

121566557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117406785-A-G

121566590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117406819-G-A

121566603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117406832-T-C

121566945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117407274-A-G

121567072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117407429-A-G

121567253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117407665-T-G

121567297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117407707-C-T

121567445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117407867-C-T

121567768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408244-G-A

http://identifiers.org/hco/1/GRCh38#121567783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117408258-A-C

121567836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408306-G-C

121567864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408333-G-A

121567985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408421-A-G

http://identifiers.org/hco/1/GRCh38#121568040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117408475-C-A

121568040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408475-C-T

121568041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408476-T-C

121568042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408477-G-C

121568042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408477-G-T

121568141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 117408575-G-A

121568141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 117408575-G-C

121568141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 117408575-G-T

121568142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 117408576-T-C

121568189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117408623-G-A

121568189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: non coding transcript exon variant
orthologous variants: 117408623-G-T

121568216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408650-A-G

121568350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117409038-A-T

121568404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117409179-C-T

http://identifiers.org/hco/1/GRCh38#121568631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117409454-C-A

121568631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117409454-C-G

121568839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117409647-G-A

121568839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117409647-G-T

http://identifiers.org/hco/1/GRCh38#121568915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117409697-C-A

121568915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117409697-C-G

121568915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117409697-C-T

121569162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117409945-T-C

121569392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117410146-A-T

121569479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117410226-T-C

121569549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117410305-G-A

121569549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117410305-G-T

121569556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117410312-T-C

http://identifiers.org/hco/1/GRCh38#121569845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117410561-A-C

121569955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117410655-G-A

http://identifiers.org/hco/1/GRCh38#121570023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117410750-C-A

121570042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117410769-G-T

121570160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117410898-G-A

http://identifiers.org/hco/1/GRCh38#121570197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117410936-C-A

121570280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411019-C-T

121570339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411079-G-C

121570397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411127-T-C

121570531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411200-A-G

121570577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411248-C-T

http://identifiers.org/hco/1/GRCh38#121570579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117411250-A-C

121570579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411250-A-G

http://identifiers.org/hco/1/GRCh38#121570581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117411252-C-A

121570592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411263-A-T

121570627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411294-G-T

http://identifiers.org/hco/1/GRCh38#121570671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117411337-A-C

121570771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411438-G-A

121570834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411500-T-C

http://identifiers.org/hco/1/GRCh38#121570838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117411510-C-A

121570857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411532-G-T

121570880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411555-A-T

121571002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411669-T-C

121571050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411716-G-A

121571052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411718-C-T

121571086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411752-T-G

121571267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411912-C-T

121571299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411943-G-A

121571299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411943-G-T

121571301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117411945-C-T

121571360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117412000-G-A

121571360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117412000-G-T

121571368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117412008-T-C

121571368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117412008-T-G

http://identifiers.org/hco/1/GRCh38#121571369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117412009-C-A

http://identifiers.org/hco/1/GRCh38#121571416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117412067-C-A

121571499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117412141-C-T

121571505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117412148-G-T

http://identifiers.org/hco/1/GRCh38#121571517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117412157-C-A

121571635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117412224-T-A

121571760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117412313-G-A

121571762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117412315-G-T

121571883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117412423-A-G

121572118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117412555-C-T

121572588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117412791-G-C

121572588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117412791-G-T

121572634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117412841-G-A

http://identifiers.org/hco/1/GRCh38#121572645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117412852-A-C

121572697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117412869-T-C

121572862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117412980-T-C

121572988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117413082-G-A

121573079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117413196-A-G

121573181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117413290-G-T

121573247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117413349-G-C

121573250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117413352-C-T

121573276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117413371-T-C

121573335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117413430-A-G

121573414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117413507-A-G

121573809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117413789-G-A

121573937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117413912-T-A

http://identifiers.org/hco/1/GRCh38#121573999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117413978-C-A

121574057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117414039-T-A

121574062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38661
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117414044-T-C