120763040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: 115237022-G-T

http://identifiers.org/hco/12/GRCh38#120763083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115236986-C-A

http://identifiers.org/hco/12/GRCh38#120763127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115236941-C-A

120763127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: 115236941-C-G

http://identifiers.org/hco/12/GRCh38#120763321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115236756-C-A

120763343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: 115236737-G-A

120763358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: 115236728-T-C

120763497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: 115236640-C-T

120763639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: 115236564-G-A

120763639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: 115236564-G-T

http://identifiers.org/hco/12/GRCh38#120763643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115236560-A-C

120763643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: 115236560-A-G

120763739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: 115236464-C-T

120763773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: 115236430-C-T

120764157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: 115236067-G-A

120764186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: 115236043-G-A

120764186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3 prime UTR variant
orthologous variants: 115236043-G-C

120764544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235698-T-C

120764558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235686-C-G

http://identifiers.org/hco/12/GRCh38#120764567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115235677-A-C

120764567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235677-A-G

120764567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235677-A-T

http://identifiers.org/hco/12/GRCh38#120764575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115235669-C-A

120764575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235669-C-T

http://identifiers.org/hco/12/GRCh38#120764582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115235662-C-A

120764599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235645-G-T

http://identifiers.org/hco/12/GRCh38#120764616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115235628-A-C

120764616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235628-A-T

120764623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235620-T-G

http://identifiers.org/hco/12/GRCh38#120764655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115235589-A-C

120764742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235500-A-G

http://identifiers.org/hco/12/GRCh38#120764857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115235389-C-A

120764857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235389-C-T

120764870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235376-A-G

120764871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235375-T-A

120764871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235375-T-C

120764871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235375-T-G

120764970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235281-G-A

120764984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115235267-T-C

120765075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 115235178-G-C

120766348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115233927-G-A

120767275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115233442-G-A

120767355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115233342-C-T

http://identifiers.org/hco/12/GRCh38#120767377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115233325-C-A

120767377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115233325-C-G

120768282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115227099-G-A

120768282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115227099-G-T

120768533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115226839-A-G

120768533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115226839-A-T

120768564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115226808-T-A

120768584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115226784-G-T

http://identifiers.org/hco/12/GRCh38#120768670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115226736-A-C

120768670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226736-A-G

120768670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226736-A-T

http://identifiers.org/hco/12/GRCh38#120768673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115226733-C-A

120768673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226733-C-T

120768680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226727-T-A

120768680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226727-T-C

120768680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226727-T-G

http://identifiers.org/hco/12/GRCh38#120768700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115226692-C-A

120768700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226692-C-T

http://identifiers.org/hco/12/GRCh38#120768715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115226678-C-A

120768715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226678-C-G

120768715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226678-C-T

120768716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226677-T-A

120768716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226677-T-C

120768716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226677-T-G

http://identifiers.org/hco/12/GRCh38#120768723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115226670-C-A

120768723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226670-C-T

http://identifiers.org/hco/12/GRCh38#120768765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115226638-C-A

120768766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226637-T-C

120768828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226579-T-C

120768893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226503-G-T

120768896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226500-T-A

120768896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226500-T-C

120768930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226466-G-A

120768930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226466-G-C

120768930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115226466-G-T

120782604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115223071-T-C

120782604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115223071-T-G

120782610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115223065-A-G

120782792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115222890-G-A

120782792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115222890-G-C

120782792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115222890-G-T

120782832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115222846-G-A

120782832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115222846-G-T

120782848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115222827-T-A

120782858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115222817-T-C

120782858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115222817-T-G

120782863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115222814-G-A

120783152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, undefined
orthologous variants: 115221944-T-C

120783297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115221823-G-A

120783650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115221584-A-G

120783650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115221584-A-T

120783658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115221576-A-G

120783658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115221576-A-T

120783800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115221421-G-T

120784118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115220610-G-T

120784148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115220580-A-G

120784193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115220544-A-G

120784266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115220477-G-A

120784286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115220467-G-A

120784286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115220467-G-T

120784403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115220431-T-G

120786047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115218237-G-T

120786164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115218111-T-C

120786256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115218038-G-A

120786256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115218038-G-T

120786263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115218031-T-C

120789956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115214117-T-C

http://identifiers.org/hco/12/GRCh38#120790085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115214002-A-C

120790181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115213918-T-G

120790207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115213893-G-A

120791434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115212994-T-C

120791625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115212807-A-G

http://identifiers.org/hco/12/GRCh38#120791626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115212806-C-A

120791626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115212806-C-T

http://identifiers.org/hco/12/GRCh38#120791722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115212740-C-A

http://identifiers.org/hco/12/GRCh38#120791872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115212615-C-A

120791872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 115212615-C-T

120798611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115209848-T-A

120798611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115209848-T-C

120798611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115209848-T-G

120798874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115209627-T-C

120798956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115209542-G-A

120799040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115209479-C-G

120799861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115208609-G-A

120800039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115208432-G-C

120800108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115208364-T-C

120808660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115202234-A-G

120808761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115202136-T-C

120808779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115202118-A-G

120808824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115202042-A-G

120808883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115201987-T-C

120809698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115200791-T-C

120809757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115200732-C-G

120809815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115200681-T-C

http://identifiers.org/hco/12/GRCh38#120809879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115200625-C-A

120809879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115200625-C-G

http://identifiers.org/hco/12/GRCh38#120810671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115199799-C-A

120810671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115199799-C-T

120810888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: splice acceptor variant
orthologous variants: 115199617-T-C

120810976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115199568-G-A

120810976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115199568-G-C

120810976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115199568-G-T

http://identifiers.org/hco/12/GRCh38#120811109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115199440-C-A

120811109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115199440-C-T

120811156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115199381-T-C

120811234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115199338-G-T

120811287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115199290-G-A

120811287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115199290-G-T

http://identifiers.org/hco/12/GRCh38#120811354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115199222-C-A

120817975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115194102-A-T

http://identifiers.org/hco/12/GRCh38#120818437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115193637-A-C

120818706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115193390-T-C

http://identifiers.org/hco/12/GRCh38#120818755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115193341-A-C

120819012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115193062-C-T

120819111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115192964-G-A

120819432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115192483-G-A

120819784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115192178-T-A

120819818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115192143-G-A

http://identifiers.org/hco/12/GRCh38#120821245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115190112-C-A

120821461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115189929-G-A

120821528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115189868-T-A

120821619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115189806-T-C

http://identifiers.org/hco/12/GRCh38#120821636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115189789-C-A

120822871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115189214-C-G

120837194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115184563-C-T

120841933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115181342-G-C

http://identifiers.org/hco/12/GRCh38#120846438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115179670-A-C

120846665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115179198-T-A

120847853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, undefined
orthologous variants: 115178519-C-G

120847936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron_variant, undefined
orthologous variants: 115178453-A-G

120847968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115178424-G-A

120848638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115177419-A-G

120893639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115157098-A-G

120893714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115157042-T-C

120894035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115156738-T-C

120894314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115156692-A-G

120894500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115156633-T-C

120895621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115156161-A-T

120895842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115155874-G-A

120896353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115155474-A-G

120896435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115155397-T-C

120897152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115154805-T-C

120898825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115153632-T-C

120899095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115153381-T-A

http://identifiers.org/hco/12/GRCh38#120899107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115153369-C-A

120899505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115152612-G-C

120899550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115152573-T-C

120899585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115152538-T-C

120899585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115152538-T-G

120901612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115151643-G-A

120901612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115151643-G-C

120901612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115151643-G-T

120901619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115151636-G-C

120901879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 115151374-T-C

120902224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115150977-G-C

120902224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115150977-G-T

120902625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115150614-A-G

120903188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115150041-T-C

http://identifiers.org/hco/12/GRCh38#120903253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115149983-C-A

120903253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115149983-C-T

http://identifiers.org/hco/12/GRCh38#120903306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115149966-C-A

120903306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115149966-C-T

120903473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115149842-A-G

http://identifiers.org/hco/12/GRCh38#120903523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115149789-C-A

120903523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115149789-C-T

http://identifiers.org/hco/12/GRCh38#120903724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115149738-C-A

120903724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115149738-C-T

120903750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115149726-G-A

120903750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115149726-G-C

120903750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: intron variant
orthologous variants: 115149726-G-T

120903982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149574-T-A

120903982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149574-T-C

120903982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149574-T-G

http://identifiers.org/hco/12/GRCh38#120903983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115149573-C-A

120903983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149573-C-G

120903983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149573-C-T

http://identifiers.org/hco/12/GRCh38#120904035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115149533-C-A

http://identifiers.org/hco/12/GRCh38#120904046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115149522-A-C

120904046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149522-A-G

120904046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149522-A-T

http://identifiers.org/hco/12/GRCh38#120904048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#115149521-C-A

120904048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149521-C-T

120904061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149508-T-A

120904061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149508-T-C

120904061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149508-T-G

120904112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149450-G-A

120904112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149450-G-C

120904112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149450-G-T

120904169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149390-A-G

120904303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 115149255-T-A

120904303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 115149255-T-C

120904303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 115149255-T-G

120904320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149238-G-A

120904320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149238-G-C

120904320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30424
most severe consequence: 5 prime UTR variant
orthologous variants: 115149238-G-T