84009682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120207414-T-A

84009682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120207414-T-C

http://identifiers.org/hco/16/GRCh38#84009704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120207437-C-A

84009704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120207437-C-G

84009707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120207440-C-T

http://identifiers.org/hco/16/GRCh38#84009802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120207506-C-A

84009802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120207506-C-G

84009802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120207506-C-T

84009808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120207512-C-G

84009808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120207512-C-T

http://identifiers.org/hco/16/GRCh38#84010792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120208186-C-A

84010792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208186-C-G

84010792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208186-C-T

84010841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208221-A-T

84010896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208274-C-G

84010896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208274-C-T

84011028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208576-C-T

84011044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208594-T-G

84011105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208651-A-G

84011183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208702-C-T

84011224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208716-C-G

84011224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208716-C-T

84011282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208768-C-G

84011343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208807-G-A

84011362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208824-C-T

84011405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208841-C-G

84011405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208841-C-T

84011414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208850-C-G

84011437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208873-C-T

84011493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208929-C-T

84011494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208930-C-G

84011494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208930-C-T

http://identifiers.org/hco/16/GRCh38#84012969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120209332-C-A

http://identifiers.org/hco/16/GRCh38#84013065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120209433-C-A

84013065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209433-C-G

84013065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209433-C-T

http://identifiers.org/hco/16/GRCh38#84013078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120209445-A-C

http://identifiers.org/hco/16/GRCh38#84013129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120209499-C-A

84013129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209499-C-T

84013131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209501-G-A

84013131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209501-G-C

84013146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209519-A-G

84013146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209519-A-T

http://identifiers.org/hco/16/GRCh38#84013185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120209546-C-A

http://identifiers.org/hco/16/GRCh38#84013186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120209547-C-A

84013186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209547-C-G

84013186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209547-C-T

84013204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209566-G-A

84013263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209619-G-A

84013277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209631-G-A

84015113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120211397-T-G

84015185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120211454-C-G

http://identifiers.org/hco/16/GRCh38#84015378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120211644-A-C

84015398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120211662-G-A

84015475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120211728-T-G

84015499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120211751-G-A

84016529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120212199-G-A

84016549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120212219-T-A

84016549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120212219-T-C

84016550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120212220-G-A

84016550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120212220-G-C

84016550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120212220-G-T

84016580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120212250-G-A

84016580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120212250-G-C

84016580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120212250-G-T

http://identifiers.org/hco/16/GRCh38#84016603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120212273-C-A

84016603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120212273-C-G

84016603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120212273-C-T

84016724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120212394-T-C

http://identifiers.org/hco/16/GRCh38#84016841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120212488-C-A

84016841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120212488-C-G

84016852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120212499-G-A

84016946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120212553-G-A

84016946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120212553-G-T

http://identifiers.org/hco/16/GRCh38#84016992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120212580-C-A

84016992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120212580-C-T

84017076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120212650-G-A

84017078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120212652-T-G

84017085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120212659-C-G

84017087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120212661-G-A

84017087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120212661-G-T

http://identifiers.org/hco/16/GRCh38#84017265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120212841-A-C

84017265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: synonymous variant
orthologous variants: 120212841-A-G

84017388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120212946-T-A

84017388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120212946-T-C

84017400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120212958-T-C

84017477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213000-G-T

84017739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213208-G-A

84017739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213208-G-C

84017939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213402-C-T

http://identifiers.org/hco/16/GRCh38#84018008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120213471-C-A

84022201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213530-G-A

84022247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213569-A-T

84022314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213635-C-G

84022336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213657-C-T

84022356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213676-C-T

http://identifiers.org/hco/16/GRCh38#84022389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120213709-C-A

84022493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213773-T-C

84022493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213773-T-G

84022506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213786-G-A

84022511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213791-G-A

84022567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213845-C-T

http://identifiers.org/hco/16/GRCh38#84022637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120213909-C-A

84022637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213909-C-G

84022672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213949-T-A

84022672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213949-T-C

http://identifiers.org/hco/16/GRCh38#84022677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120213954-C-A

84022677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213954-C-G

84022677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213954-C-T

http://identifiers.org/hco/16/GRCh38#84022679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120213956-C-A

84022679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213956-C-T

84022685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213961-G-A

84022685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213961-G-C

84022685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120213961-G-T

84022748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120214018-T-C

84022749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120214019-G-A

84022749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120214019-G-C

84022749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120214019-G-T

84022833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: synonymous variant
orthologous variants: 120214103-G-A

84022833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: missense variant
orthologous variants: 120214103-G-T

84022903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120214175-G-A

84022903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120214175-G-C

84027924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120217762-C-G

84027959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120217783-T-C

http://identifiers.org/hco/16/GRCh38#84027997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120217821-A-C

84028007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120217823-C-T

84028011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120217827-T-C

84028045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120217865-A-T

84028992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120218553-C-T

84029122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120218648-G-A

84029122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120218648-G-C

84029256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120218772-G-A

84029256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120218772-G-C

84029382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120218872-G-A

84029382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120218872-G-C

84029382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120218872-G-T

84029418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120218907-A-T

84029619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120219102-G-A

84029619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120219102-G-T

84029648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120219131-T-A

84029653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120219136-G-A

84029653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120219136-G-C

84029771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120219249-C-T

84029946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120219414-A-G

84029946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120219414-A-T

84031345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120220570-G-C

84031385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120220609-T-G

84031535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120220746-C-G

84031535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120220746-C-T

http://identifiers.org/hco/16/GRCh38#84031763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120220851-C-A

84031763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120220851-C-G

84031917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: synonymous variant
orthologous variants: 120220985-C-T

http://identifiers.org/hco/16/GRCh38#84031996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120221067-C-A

84031996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120221067-C-T

http://identifiers.org/hco/16/GRCh38#84032057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120221112-C-A

84032057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120221112-C-G

84032057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120221112-C-T

84032071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120221118-A-G

84032100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120221148-T-A

84032100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120221148-T-C

http://identifiers.org/hco/16/GRCh38#84032111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120221160-A-C

84032111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120221160-A-G

84032111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120221160-A-T

http://identifiers.org/hco/16/GRCh38#84032113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120221162-C-A

84032113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120221162-C-T

http://identifiers.org/hco/16/GRCh38#84032119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120221168-A-C

84032119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120221168-A-G

84032119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120221168-A-T

84032144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120221192-T-G

http://identifiers.org/hco/16/GRCh38#84033317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120222785-C-A

84033317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120222785-C-G

84033317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120222785-C-T

84033348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: synonymous variant
orthologous variants: 120222820-G-A

84033348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: missense variant
orthologous variants: 120222820-G-C

84033348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: synonymous variant
orthologous variants: 120222820-G-T

84033408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: synonymous variant
orthologous variants: 120222880-G-A

http://identifiers.org/hco/16/GRCh38#84033416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120222888-C-A

84033447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: synonymous variant
orthologous variants: 120222910-G-A

84033447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: synonymous variant
orthologous variants: 120222910-G-T

84033608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223037-T-A

84033608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223037-T-G

84033844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223207-T-C

84033899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223224-T-C

84033936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223262-T-G

84034022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223296-G-A

84034024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223298-T-C

84034025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223299-G-A

84034059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223336-G-A

84034149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223405-C-T

84034156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223417-C-T

84034166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223427-G-A

84034166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223427-G-T

84034194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223451-G-C

http://identifiers.org/hco/16/GRCh38#84034302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120223528-C-A

84034368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223572-G-A

84034426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223608-G-A

84034438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223620-A-T

84034458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223636-G-A

84034459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223637-G-A

84034459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223637-G-T

84034542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223706-G-A

84034703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223831-T-C

84034816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223938-C-G

84034853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223984-G-C

84034863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120223994-G-T

84034880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120224011-A-G

http://identifiers.org/hco/16/GRCh38#84034881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120224012-C-A

84034909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120224049-G-A

84034910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120224050-G-A

84034921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120224061-T-C

84034974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120224108-C-G

84035012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120224147-G-A

84035012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120224147-G-C

84035012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120224147-G-T

84035031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120224166-C-T

84035159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120224280-C-T

84035333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120224405-A-G

http://identifiers.org/hco/16/GRCh38#84035722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120224715-C-A

84036033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120225788-C-T

84036090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120225847-T-C

84036090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120225847-T-G

84036141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120225887-T-G

84036148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120225894-T-C

84036245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120225960-G-A

84036245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120225960-G-C

84036278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226002-T-C

84036393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226107-T-A

84036407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226121-A-T

84036475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226189-A-G

84036492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226206-T-A

http://identifiers.org/hco/16/GRCh38#84036585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120226260-C-A

84036585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226260-C-G

84036585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226260-C-T

http://identifiers.org/hco/16/GRCh38#84036588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120226263-C-A

84036588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226263-C-G

84036588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226263-C-T

84036641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226342-T-C

84036641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226342-T-G

http://identifiers.org/hco/16/GRCh38#84036644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120226345-A-C

84036644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226345-A-G

84036658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226356-G-A

84036658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226356-G-C

84036658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226356-G-T

http://identifiers.org/hco/16/GRCh38#84036662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120226360-C-A

84036662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226360-C-G

84036662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226360-C-T

84036799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 120226497-G-A

84036799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 120226497-G-T

84036832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 120226530-G-A

84036832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 120226530-G-T

84036855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 120226553-C-T

http://identifiers.org/hco/16/GRCh38#84036871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120226569-C-A

84036871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 120226569-C-G

84036871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 120226569-C-T

http://identifiers.org/hco/16/GRCh38#84036904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120226602-C-A

84036904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120226602-C-G

84036904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120226602-C-T

84036911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226609-G-A

84036911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226609-G-C

84036911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226609-G-T

84036935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226633-T-G

http://identifiers.org/hco/16/GRCh38#84036949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120226634-C-A

84036949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226634-C-G

84036949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226634-C-T

http://identifiers.org/hco/16/GRCh38#84036957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120226642-A-C

84036957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226642-A-G

84037058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226703-A-G

84037213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226811-C-T

84037261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226848-G-A

84037276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226851-G-A

84037276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226851-G-C

84037308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226877-C-G

84037373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226928-G-A

84037373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226928-G-C

84037373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226928-G-T

84037386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron variant
orthologous variants: 120226941-C-G

http://identifiers.org/hco/16/GRCh38#84041854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120227610-C-A

84041873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120227628-G-A

84041873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120227628-G-C

84041873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120227628-G-T

84041950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120227721-T-C

84041973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120227744-T-C

84042005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120227776-T-C

84042070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120227841-C-T

84042083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120227854-G-A

84042083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120227854-G-C

84042180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120227948-G-C

84042180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120227948-G-T

84042181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120227949-A-G

84042181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120227949-A-T

84042207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120227969-C-G

84042207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120227969-C-T

84042271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120228043-T-G

http://identifiers.org/hco/16/GRCh38#84042437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120228156-C-A

http://identifiers.org/hco/16/GRCh38#84042444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120228163-C-A

84042444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120228163-C-G

84042444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120228163-C-T

http://identifiers.org/hco/16/GRCh38#84042446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120228165-C-A

84042446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120228165-C-T

84042498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120228215-T-A

84042498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120228215-T-C

84042498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120228215-T-G

84042500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120228217-T-A

84042500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120228217-T-G

http://identifiers.org/hco/16/GRCh38#84042514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120228226-C-A

84042514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120228226-C-G

84042514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120228226-C-T

http://identifiers.org/hco/16/GRCh38#84042530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120228242-C-A

84042530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120228242-C-T

84042605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120228310-T-A

84042605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120228310-T-C

84042605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120228310-T-G

84042680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120228385-A-G

84042738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120228441-C-T

http://identifiers.org/hco/16/GRCh38#84042756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120228458-C-A

84042756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120228458-C-T

84042757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120228459-A-G

84042809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120228509-T-C

84042965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120228643-C-T

84042998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120228662-C-T

84043005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120228669-G-A

84043005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120228669-G-C

84043070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120228746-G-A

84043070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120228746-G-C

84043116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120228794-C-G

84043204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120228902-G-A

84043210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120228908-G-A

84043221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120228919-C-T

84043246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120228957-A-G

http://identifiers.org/hco/16/GRCh38#84043335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#120229039-C-A

84043335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32434
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120229039-C-G