958418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 31425447-A-T

958489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: non coding transcript exon variant
orthologous variants: 31425527-G-A

958489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: non coding transcript exon variant
orthologous variants: 31425527-G-T

958543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: non coding transcript exon variant
orthologous variants: 31425573-G-A

958605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31425670-T-C

958707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31425762-T-C

958844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31425887-T-G

958914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31425926-G-A

959302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31426270-C-T

959305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31426273-A-G

959340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31426308-G-A

959648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31427807-A-G

960001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31428255-A-T

960445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31428690-G-A

961091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31429327-A-T

961106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31429344-G-C

961127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31429362-G-A

961221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31429443-T-C

961546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31429811-C-T

http://identifiers.org/hco/6/GRCh38#961571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31429835-A-C

962967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31430682-G-T

963259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31431001-G-C

963336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31431073-G-A

963427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31431162-G-A

963428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31431163-T-G

963583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31431305-C-T

963910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31431815-C-T

964525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31432443-C-T

964572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31432646-T-C

964589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31432663-G-T

964643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31432716-G-A

964742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31432809-A-G

964970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31433197-G-A

965206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31433421-T-A

965377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31433523-T-C

965377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31433523-T-G

http://identifiers.org/hco/6/GRCh38#965744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31433869-A-C

965787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31433897-G-A

965887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31433928-C-T

965962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31433965-A-G

966001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31434016-T-C

966004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31434019-C-G

966004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31434019-C-T

966033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31434048-T-C

966033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31434048-T-G

966114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31434136-G-A

966343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

966404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31434284-C-T

966439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31434320-A-G

966478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31434339-G-C

966660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31434433-C-T

966913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31434495-A-G

967012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31434586-G-A

967013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31434587-G-A

967087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31434670-T-A

967087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31434670-T-C

http://identifiers.org/hco/6/GRCh38#967636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31435183-C-A

967685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31435239-A-G

967932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31435957-G-A

968171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31436305-C-T

968172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31436306-A-G

968897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31436975-A-G

968946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437021-T-G

969028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437108-C-T

969050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437130-G-T

969158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437244-G-A

969158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437244-G-T

969233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437305-C-T

969415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437486-A-T

969443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437516-G-T

http://identifiers.org/hco/6/GRCh38#969446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31437519-A-C

969446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437519-A-G

969446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437519-A-T

969453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437526-C-T

969454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437527-T-C

969517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437570-C-T

969565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437613-C-T

969717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437676-A-G

969718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31437677-T-C

970022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31438000-T-A

970022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31438000-T-G

970081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31438059-A-G

970274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31438241-T-C

970489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31438463-A-G

971049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31439129-A-G

971053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31439133-T-C

971362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31439460-T-C

971413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31439510-G-C

971631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31439696-C-T

971734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31439782-G-C

972055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31440093-C-G

http://identifiers.org/hco/6/GRCh38#972179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31440164-C-A

972179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31440164-C-G

http://identifiers.org/hco/6/GRCh38#972432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31440366-A-C

972583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31440478-C-T

972605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31440488-T-C

972736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31440620-T-A

http://identifiers.org/hco/6/GRCh38#973169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31440724-A-C

980403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31443185-T-C

http://identifiers.org/hco/6/GRCh38#981236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31444256-C-A

981296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31444316-G-A

981754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31444738-C-G

http://identifiers.org/hco/6/GRCh38#981798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31444787-A-C

981817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31444806-G-C

981826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31444812-C-G

981826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31444812-C-T

981881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31444867-C-T

984139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31446477-G-A

984198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31446536-C-T

984284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31446608-C-T

984532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31446826-C-T

984687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31446976-T-A

984792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31447062-C-T

984793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31447063-G-A

984995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31447255-T-C

1001275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31451376-A-G

http://identifiers.org/hco/6/GRCh38#1001284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31451385-A-C

1001284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31451385-A-G

1001290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31451389-C-T

1001508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31451605-A-G

1001517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31451614-G-T

1001616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31451947-T-A

1001664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31451985-G-A

1001664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31451985-G-C

1001696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31452008-C-G

1001825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31452135-C-T

1001826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31452136-G-A

1001829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31452139-T-C

1001832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31452142-G-A

1001845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31452155-T-G

http://identifiers.org/hco/6/GRCh38#1001849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31452159-C-A

1001940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31452273-T-G

http://identifiers.org/hco/6/GRCh38#1002194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31452509-A-C

1002237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31452552-C-T

1002238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31452553-G-C

http://identifiers.org/hco/6/GRCh38#1002420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31452787-C-A

1002420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31452787-C-T

1007857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457376-C-T

1007899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457420-C-T

1007989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457503-A-T

1008083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457585-C-G

http://identifiers.org/hco/6/GRCh38#1008180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31457679-A-C

1008180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457679-A-G

1008205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457698-G-A

1008214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457707-A-T

1008254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457745-A-T

1008310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31457795-T-C

1010528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31458400-C-G

1010546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31458418-C-T

1010551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31458423-T-C

1010560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31458432-C-T

http://identifiers.org/hco/6/GRCh38#1010612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31458489-C-A

1010685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31458566-G-A

1010967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31458798-G-T

1011169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31458964-C-T

1011198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31458993-G-A

1011367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459157-C-T

1011546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459331-G-A

1011631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459407-C-T

1011701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459470-G-A

1012918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459621-C-G

1012999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459684-G-A

1013013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459698-T-G

1013027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459712-T-C

1013158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459832-C-G

1013158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31459832-C-T

1013450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31460148-C-T

1014254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31460998-G-A

1015826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31461811-C-T

1015846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31461831-C-T

http://identifiers.org/hco/6/GRCh38#1015852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31461836-C-A

1015856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31461840-A-G

1015857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31461841-G-T

1015860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31461844-A-G

1016019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462011-G-T

1016026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462018-C-T

1016133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462114-C-T

1016342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462337-G-A

1016382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462374-C-T

1016493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462486-G-A

1016493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462486-G-C

http://identifiers.org/hco/6/GRCh38#1016631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31462622-C-A

1016704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31462694-T-C

1016900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31464573-A-G

1016922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31464599-T-C

1016947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31464624-T-C

http://identifiers.org/hco/6/GRCh38#1016982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31464669-A-C

1017391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31465285-T-C

1017599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31465483-C-T

1017695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31465652-T-G

1017708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31465672-G-A

1017890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31465853-C-T

1017943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31465902-C-T

1017963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31465923-C-T

1018083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31466037-T-C

1018479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31466472-G-T

1018553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31466550-A-G

http://identifiers.org/hco/6/GRCh38#1018678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31466668-C-A

1018678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31466668-C-T

1018693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31466682-A-T

1018733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31466726-T-C

1018890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31466885-T-A

1018981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31466956-C-T

1019123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31467064-A-G

http://identifiers.org/hco/6/GRCh38#1019127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31467068-C-A

1023776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31472564-T-A

1024017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31472806-T-G

1024426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31473369-C-T

1024491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31473428-T-A

1024491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31473428-T-C

http://identifiers.org/hco/6/GRCh38#1024582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31473516-C-A

1024633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31473553-C-T

1024635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31473557-C-T

http://identifiers.org/hco/6/GRCh38#1024745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#31473651-C-A

1024907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31473806-G-C

1025296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31474190-T-G

1025302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31474196-T-A

1025426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31474329-T-C

http://identifiers.org/hco/6/GRCh38#1025480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31474390-C-A

1026029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31476448-T-C

1026092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31476495-C-T

http://identifiers.org/hco/6/GRCh38#1026386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31476766-C-A

1026537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31476922-A-G

1026537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31476922-A-T

http://identifiers.org/hco/6/GRCh38#1026558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31476943-A-C

1026558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31476943-A-G

1026558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31476943-A-T

1026562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31476947-G-T

1026870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477226-A-G

1026870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477226-A-T

1026885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477241-G-A

1026957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477301-T-C

http://identifiers.org/hco/6/GRCh38#1026958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31477302-C-A

1026979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477323-G-A

1026979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477323-G-T

1026983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477327-G-A

1026983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477327-G-T

1026991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477335-G-A

1026991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477335-G-C

1026991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477335-G-T

1027006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477347-A-T

1027066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477401-G-A

1027103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477440-G-A

1027103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477440-G-T

1027175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31477479-G-T

http://identifiers.org/hco/6/GRCh38#1027233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31477537-C-A

http://identifiers.org/hco/6/GRCh38#1027265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31477559-C-A

http://identifiers.org/hco/6/GRCh38#1027280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31477574-A-C

1027296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31477591-G-A

1027296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31477591-G-T

1027423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31477718-C-T

1027443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31477738-G-A

1027585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31477883-A-G

1027616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31477911-T-C

1027616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31477911-T-G

http://identifiers.org/hco/6/GRCh38#1027664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31477953-A-C

1028222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31478460-G-A

1028501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31478694-T-C

1028671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31478855-G-T

1034687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31483215-C-T

1034890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31483406-T-C

1035277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31483778-A-T

1035336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31483832-G-A

1035357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31483853-C-G

1035361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31483857-C-G

1035369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31483863-T-C

1035425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31483903-G-T

1035485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31483956-G-A

1035846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31484084-G-A

http://identifiers.org/hco/6/GRCh38#1036190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31484383-A-C

1036190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31484383-A-T

1036195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31484388-A-G

1036364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31484564-G-A

1036560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31486452-C-T

1038140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31487378-C-T

1038242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31487492-T-C

1038317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31487563-T-C

1038413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31487666-A-G

1038437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31487682-A-G

1038454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31487699-G-C

1038927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31488124-A-G

1039498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31488656-C-T

1039759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31488826-C-T

1039809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31488874-G-A

1040038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31489096-G-A

1040039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31489097-A-G

1040188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31489874-C-T

http://identifiers.org/hco/6/GRCh38#1040235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31489899-A-C

1040305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31489939-A-T

1040582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31490185-G-A

1040582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31490185-G-C

1040796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31490334-C-T

1040974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31490485-C-T

1043349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31492167-G-A

1043493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31492296-T-G

1043578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31492376-G-A

1043578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31492376-G-C

http://identifiers.org/hco/6/GRCh38#1043841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31492606-C-A

1043877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31492646-A-T

1043945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31492743-C-T

1044025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31492818-G-A

1044036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31492829-T-C

1044189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31492960-T-C

1044191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31492962-G-A

1044437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31493157-T-C

1044769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31493470-G-A

1044969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31493626-A-T

1044992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31493648-T-G

1045037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31493689-G-A

1045071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31493696-A-G

1045191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31493811-A-G

http://identifiers.org/hco/6/GRCh38#1045287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31493896-C-A

http://identifiers.org/hco/6/GRCh38#1045352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31493947-C-A

1045480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31494070-A-G

http://identifiers.org/hco/6/GRCh38#1045767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31494356-A-C

1047600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31497245-A-G

1047609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31497254-G-A

1047928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31497539-C-T

1048323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31497908-C-G

1048485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31498066-A-G

1048627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31498228-C-T

1048648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31498260-C-T

1048651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31498263-T-A

1049228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31499145-T-C

1049228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31499145-T-G

1049358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31499255-T-C

1052323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31501817-C-T

1052492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31502012-A-T

1052619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31502136-C-T

1054381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31503243-C-T

1054419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31503280-T-C

1054682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31505207-C-T

1054691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31505216-G-A

http://identifiers.org/hco/6/GRCh38#1054725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#31505250-A-C

1054943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31505435-G-T

1054955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31505444-G-A

1055385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31505830-A-T

1055551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31505956-G-A

1057928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31506141-C-T

http://identifiers.org/hco/6/GRCh38#1058161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31506500-C-A

1058284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31506618-A-G

1063000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31510602-G-T

1063006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31510608-C-T

1063081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31510672-G-A

1063081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31510672-G-C

1063153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31510740-G-A

1063267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31510841-C-T

1063445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31511070-C-T

1063474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31511148-T-C

1063556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31511219-G-A

1063720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31511348-C-T

http://identifiers.org/hco/6/GRCh38#1063755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31511383-C-A

1064205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31511883-C-G

1064240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31511920-C-T

1064651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31512728-T-C

1065082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31513122-C-G

1065782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31513588-T-C

1065867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31513675-A-G

1065895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31513703-A-T

1066263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31514015-T-A

1066371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31514194-A-T

1066410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31514273-C-T

http://identifiers.org/hco/6/GRCh38#1066588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31514451-C-A

1066666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31514514-C-T

1066708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31514554-G-A

1066715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31514561-A-G

1066841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31514697-A-G

http://identifiers.org/hco/6/GRCh38#1066909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31514763-A-C

1067012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31514863-T-C

1067175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31515095-C-T

1067267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31515194-C-T

http://identifiers.org/hco/6/GRCh38#1067308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31515236-A-C

1067445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31515350-G-C

1067445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31515350-G-T

1067561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31515415-G-A

http://identifiers.org/hco/6/GRCh38#1067574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31515428-C-A

1067574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31515428-C-T

1068146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31516009-T-A

1068153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31516016-G-C

1068250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31516119-T-C

1068449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31516294-T-G

http://identifiers.org/hco/6/GRCh38#1068467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31516312-C-A

1068470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31516315-T-G

1068632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31516470-T-G

1068765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31516607-A-G

1075633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31519862-T-G

1075987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31520180-A-G

1076034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31520226-G-A

1076077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31520271-G-C

1076086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31520280-T-C

1077142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31520650-C-G

1077256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31520756-G-C

1077263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31520763-G-A

1077368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31520815-T-G

1077371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31520818-G-A

1077540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31520958-A-G

1077582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31521000-T-G

1077644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31521063-T-C

1078038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31521451-G-T

1078840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31522954-T-C

1078972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31523086-T-G

1078994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31523108-C-T

http://identifiers.org/hco/6/GRCh38#1079532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31523437-A-C

1079532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31523437-A-G

1079537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31523445-T-A

1079537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31523445-T-C

1079863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31523760-T-C

1080339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31523966-C-T

1080532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31524139-G-A

1080747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31524346-T-C

1081088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31524661-C-G

http://identifiers.org/hco/6/GRCh38#1081106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31524679-A-C

1081123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31524714-T-C

1081159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31524750-C-T

http://identifiers.org/hco/6/GRCh38#1081388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31524992-A-C

1081592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31525169-C-T

http://identifiers.org/hco/6/GRCh38#1081596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31525173-C-A

1081636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31525212-T-C

http://identifiers.org/hco/6/GRCh38#1081884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31525432-A-C

http://identifiers.org/hco/6/GRCh38#1081890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31525438-A-C

1081890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31525438-A-G

1081897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31525445-T-C

1081914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31525461-T-C

1081955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31525493-T-C

1081986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31525526-G-A

1082411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31525906-G-T

1082412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31525907-C-T

1082485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31525974-T-C

1082733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31526222-G-A

1082747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31526236-A-G

1082974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31526673-T-A

1083133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31526828-C-T

1083489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31527546-G-A

1083654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31527661-A-G

1084697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31528031-A-G

1085169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31528479-G-A

1085169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31528479-G-T

1085612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31530078-G-C

1085630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31530113-T-C

1085639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31530122-A-G

http://identifiers.org/hco/6/GRCh38#1085701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31530172-C-A

1090951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31532685-A-G

1091011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31532745-G-A

1091728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31533586-A-G

1091828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31533684-G-A

1091828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31533684-G-C

1092164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31533924-A-G

1094548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31535898-A-T

1094640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31536012-A-G

http://identifiers.org/hco/6/GRCh38#1094712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#31536100-C-A

1094712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31536100-C-T

1094758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31536146-C-T

1094984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31536370-G-A

1094990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31536376-A-G

1098287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31544918-A-T

1098319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31544950-C-T

1098536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31545178-A-G

1098993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31545604-T-C

1099492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31546568-G-A

1100936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31549439-G-T

1100955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31549458-T-G

1100980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27768
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31549482-G-A