95752031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76061807-G-A

http://identifiers.org/hco/5/GRCh38#95752114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76061718-C-A

95752114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76061718-C-T

95752174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76061654-G-A

95752185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76061633-T-A

95752185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76061633-T-C

95752185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76061633-T-G

95752188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76061624-T-G

95752196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76061613-T-A

95752196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76061613-T-C

95752202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76061607-T-C

95752386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76061441-A-G

95752398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76061429-G-T

95752426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76061408-T-C

95752436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76061398-C-T

95754199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76060294-G-T

95754251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76060242-G-A

95754251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76060242-G-T

95754260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76060233-A-G

95754459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76060055-C-G

95754692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76059817-G-A

95754774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76059686-G-A

95755256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76059226-G-A

95755256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76059226-G-C

95755264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76059218-A-G

95755264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76059218-A-T

95755301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76059189-A-T

95755360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76059148-A-G

95755473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76059035-G-A

95755473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76059035-G-T

http://identifiers.org/hco/5/GRCh38#95755560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76058948-C-A

95755600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76058908-C-G

95755672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76058836-A-T

95755790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76058730-A-G

http://identifiers.org/hco/5/GRCh38#95755828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76058692-C-A

95755828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76058692-C-T

http://identifiers.org/hco/5/GRCh38#95755866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76058652-C-A

95755866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76058652-C-T

95755880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76058638-T-A

95755880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76058638-T-C

95755948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76058570-A-G

http://identifiers.org/hco/5/GRCh38#95755950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76058568-A-C

http://identifiers.org/hco/5/GRCh38#95755959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76058559-C-A

95755959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76058559-C-T

95755992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76058542-T-A

95756016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76058519-T-A

http://identifiers.org/hco/5/GRCh38#95756042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76058493-C-A

95756049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76058486-C-T

95756060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76058475-A-G

95756064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76058471-C-T

http://identifiers.org/hco/5/GRCh38#95756124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76058401-A-C

95756142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76058380-C-T

http://identifiers.org/hco/5/GRCh38#95757661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76057343-A-C

95757662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76057342-C-T

95757767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76057261-A-G

95758076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76056957-T-C

95758275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76056752-C-T

95758310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76056720-A-G

95758439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76056599-G-A

95758595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76056457-G-A

95759336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76055874-C-G

95759354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76055857-A-G

http://identifiers.org/hco/5/GRCh38#95759579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76055629-A-C

95759781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76055458-G-A

95759781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76055458-G-T

95759844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76055403-G-C

95759890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76055352-T-C

95759916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76055326-A-G

95760016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76055243-C-T

95760226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76055042-G-A

95760336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76054973-T-G

95760383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76054928-C-G

95760417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76054898-C-T

95760619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76054703-A-G

95760734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76054635-T-A

95760797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76054571-C-T

95760798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76054570-G-A

95760798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76054570-G-T

95760985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76054422-G-A

95760986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76054421-T-G

95761124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76054312-G-A

http://identifiers.org/hco/5/GRCh38#95761910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76053186-A-C

95761910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76053186-A-G

95762047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76053049-G-C

95762047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76053049-G-T

95762384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76052500-G-A

95762384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76052500-G-C

95762432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76052446-G-A

95762646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76052221-A-G

95762647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76052216-T-C

95762759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76051391-A-G

95762792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76051358-G-A

95763384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76050534-G-A

95763447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76050467-A-G

95763447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76050467-A-T

http://identifiers.org/hco/5/GRCh38#95763464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76050449-C-A

95763464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76050449-C-T

95763476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, undefined
orthologous variants: 76050437-G-A

95763631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76050284-T-C

http://identifiers.org/hco/5/GRCh38#95763674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76050263-C-A

http://identifiers.org/hco/5/GRCh38#95763732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76050205-A-C

95763742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76050195-T-A

http://identifiers.org/hco/5/GRCh38#95764261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76049931-A-C

95764261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76049931-A-G

95764298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76049895-C-T

95764340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76049859-A-G

95764431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76049768-T-C

95764465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76049734-T-C

95764561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76049653-T-G

95764852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76042873-G-A

95765187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76042654-A-T

95765249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76042603-A-G

http://identifiers.org/hco/5/GRCh38#95766020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76042233-C-A

95766034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76042221-T-C

95766065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76042194-T-G

95766222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76042053-A-G

95767849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, missense_variant
orthologous variants: 76041303-G-A

95767849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, missense_variant
orthologous variants: 76041303-G-C

95767881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76041270-G-A

95767957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76041206-T-C

95767957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76041206-T-G

95768013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76041177-A-G

95768625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76040705-G-T

95768656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76040683-A-G

95768716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76040622-A-G

http://identifiers.org/hco/5/GRCh38#95771267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76040414-A-C

95771267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76040414-A-G

95771340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76040342-T-G

95771560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76040137-A-G

95771618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76040077-A-G

95771681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76040007-A-T

95771687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76040003-C-T

95772024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76039714-C-T

95772328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76039420-A-G

95772460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76033325-A-G

95772486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76033283-C-T

95772525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76033240-G-A

95773010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76033041-T-A

95773010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76033041-T-C

95773049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76032981-G-A

95776426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76031157-A-G

95776701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76030914-G-A

95777043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76030524-T-C

95777287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76030331-A-G

95777424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76030203-T-C

95778848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76028835-G-A

http://identifiers.org/hco/5/GRCh38#95779144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76028576-C-A

95779191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76028527-G-A

95779274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76028451-C-T

95779607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76027662-G-A

95779607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76027662-G-T

95779875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 76027436-T-G

95780478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76026864-C-T

95780484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76026858-T-G

95780644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76026709-C-T

95781201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76026239-G-T

95782086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76025972-T-C

95783761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76025690-A-G

95783996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76025458-T-C

95783996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76025458-T-G

95784076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76025383-A-G

http://identifiers.org/hco/5/GRCh38#95784083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76025376-C-A

95784199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76025287-T-A

95784271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76025218-A-G

95784340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76025173-G-A

95784340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76025173-G-T

95784418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76025090-T-C

http://identifiers.org/hco/5/GRCh38#95789047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76024100-C-A

95789199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76023962-C-T

95789274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76023884-T-G

95790272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76022867-T-C

95790576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76022616-G-A

95790904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76022367-T-C

95791081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76022245-T-C

95791114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76022222-T-C

95791268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76021941-C-T

95791297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76021911-T-C

95791303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76021905-A-G

95791449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76021752-G-A

http://identifiers.org/hco/5/GRCh38#95793229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76020413-C-A

http://identifiers.org/hco/5/GRCh38#95793402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76020258-C-A

95793402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76020258-C-T

95793403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76020257-T-A

95793403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76020257-T-C

http://identifiers.org/hco/5/GRCh38#95793420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76020240-C-A

95793504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76020158-G-A

95793504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76020158-G-T

95793535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76020127-T-C

95793557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76020105-G-A

95793557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76020105-G-T

95793682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76019989-C-G

95793738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76019944-A-G

http://identifiers.org/hco/5/GRCh38#95793847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76019873-C-A

http://identifiers.org/hco/5/GRCh38#95793864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76019856-C-A

http://identifiers.org/hco/5/GRCh38#95793872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76019848-A-C

95793913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76019802-A-G

95793969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76019733-G-T

95793979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76019606-C-G

95794055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76019501-C-T

95794119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76019440-T-A

95794131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76019428-T-G

http://identifiers.org/hco/5/GRCh38#95794378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76019181-C-A

95794378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76019181-C-T

95794463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76019116-T-G

95794508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76019072-A-G

95794573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76019011-A-G

95794666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76018923-T-G

95794668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76018921-G-T

95795248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76018674-G-T

95795492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76018454-G-T

95795543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76018402-T-C

95795551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76018394-A-T

95795721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76018289-G-T

95796110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76017904-G-A

95796576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76017444-T-C

95796749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76016918-A-G

95796783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76016891-A-G

95796856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76016826-T-C

95797119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76016577-T-A

95797210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76016497-G-A

95797750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76015954-T-C

95799025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76015530-T-G

95800360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76014788-G-A

95800360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76014788-G-T

http://identifiers.org/hco/5/GRCh38#95800550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76014660-A-C

95800567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76014636-A-T

95800705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76014534-A-G

95801519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76013296-T-G

95802651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76008406-A-G

http://identifiers.org/hco/5/GRCh38#95802898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76008262-A-C

95802997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76008163-A-T

95803098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76008055-G-A

95803098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76008055-G-T

95803211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76007952-T-C

95803267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76007898-G-A

95803450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76007733-G-A

http://identifiers.org/hco/5/GRCh38#95803774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76006577-C-A

95803812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76006540-A-G

http://identifiers.org/hco/5/GRCh38#95803813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#76006539-C-A

95803813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76006539-C-T

95803873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76006488-G-A

95803929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76006438-C-G

95807275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76000510-T-A

95807379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76000408-G-A

95807472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76000326-T-C

95808197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75999922-C-T

95808260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75999853-G-A

95808263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75999850-C-T

95808365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75999768-C-T

95808553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75999549-T-C

95814016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75998230-G-T

http://identifiers.org/hco/5/GRCh38#95814022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#75998224-A-C

95814119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75998096-C-G

http://identifiers.org/hco/5/GRCh38#95814172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#75998057-C-A

95814172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75998057-C-T

95814190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75998041-G-T

95814253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75997977-G-T

95814254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75997976-A-G

95814254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75997976-A-T

http://identifiers.org/hco/5/GRCh38#95814306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#75997929-C-A

95814306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75997929-C-G

http://identifiers.org/hco/5/GRCh38#95814313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#75997918-C-A

95814313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75997918-C-T

95814614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75997636-T-C

95814923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75997419-A-G

95815170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75996963-C-T

http://identifiers.org/hco/5/GRCh38#95815192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#75996946-A-C

95815333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75996803-G-A

95815632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75996533-C-T

http://identifiers.org/hco/5/GRCh38#95815898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#75996119-C-A

95815898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75996119-C-G

95816025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75995955-T-C

95816035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75995938-T-C

95816056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75995902-C-G

95816056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75995902-C-T

http://identifiers.org/hco/5/GRCh38#95816357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#75995536-A-C

95816357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75995536-A-G

95816357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75995536-A-T

95816368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75995525-G-A

95816368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75995525-G-C

95816368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75995525-G-T

95816391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75995502-T-A

95816391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75995502-T-C

95816391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75995502-T-G

95816465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75995444-G-A

95816465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75995444-G-C

95816465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75995444-G-T

95816638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75995275-C-G

95816638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75995275-C-T

95816785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75995170-G-T

95816789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75995159-T-A

95816789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75995159-T-C

95817458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994382-G-T

95817532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994294-T-C

95817532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994294-T-G

95817581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994244-T-A

95817581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994244-T-C

95817589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994240-C-T

95817596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994233-T-C

http://identifiers.org/hco/5/GRCh38#95817616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#75994211-C-A

95817616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75994211-C-T

95817711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994105-G-A

95817711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994105-G-C

http://identifiers.org/hco/5/GRCh38#95817712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#75994104-C-A

http://identifiers.org/hco/5/GRCh38#95817735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#75994060-C-A

95817735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994060-C-T

95817744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994051-G-A

95817744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994051-G-T

http://identifiers.org/hco/5/GRCh38#95817747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#75994048-C-A

95817747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994048-C-T

95817751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994044-G-A

95817751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994044-G-T

95817799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75994009-G-T

95817812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75993996-G-A

95817812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75993996-G-T

95817867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75993952-A-G

95817886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75993932-A-G

95817909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75993909-G-T

95817954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75993864-T-C

95817963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75993850-G-C

95817963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75993850-G-T

95818784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75991589-T-C

95819161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75991254-T-C

95819306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75991126-G-T

95819534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75990961-A-G

95819563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75990936-G-A

http://identifiers.org/hco/5/GRCh38#95819572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#75990927-C-A

95819572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75990927-C-T

95821380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75990131-T-C

95821489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75990043-A-G

95821543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75989989-T-C

95821812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75988932-G-A

http://identifiers.org/hco/5/GRCh38#95821828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#75988912-A-C

http://identifiers.org/hco/5/GRCh38#95822133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#75988602-A-C

95822234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75988512-G-A

95822234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75988512-G-T

95822305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 75988451-T-C

http://identifiers.org/hco/5/GRCh38#95822352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#75988412-C-A

95822352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 75988412-C-T

95822373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: 75988388-A-G

http://identifiers.org/hco/5/GRCh38#95822375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#75988386-C-A

95822689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4330
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 75988058-A-G