108382745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49018009-G-T

108382814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49017995-C-T

108390184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49006022-G-A

108390249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49005957-A-G

108390269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49005937-G-A

108390836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49004269-A-T

108390911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49004194-T-C

108391019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49004074-C-T

108391104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49003994-C-T

108391128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49003969-T-A

108391183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49003914-G-A

http://identifiers.org/hco/3/GRCh38#108391249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49003854-A-C

108395317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48996386-A-G

108400338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48990289-T-C

108407867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48983860-G-A

108408036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48983706-C-G

108408122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48983621-A-G

108408124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48983619-G-A

108408160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48983605-C-T

108408163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48983602-G-C

108408163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48983602-G-T

108408181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48983588-T-C

108408205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48983568-T-C

108408224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48983553-T-A

108408224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48983553-T-C

108408242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48983535-T-C

108409940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48981003-T-G

108410965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979987-G-A

108410965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979987-G-C

108411020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979960-G-A

108411035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979946-G-A

108411035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979946-G-T

108411077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979922-T-A

108411077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979922-T-C

108411130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979891-T-G

108411152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979868-C-T

http://identifiers.org/hco/3/GRCh38#108411783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48979273-A-C

108411795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979261-G-A

http://identifiers.org/hco/3/GRCh38#108411900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48979160-A-C

108411939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979118-C-T

108412068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979017-G-C

108412086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979003-T-C

108417001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973749-G-T

108417014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973736-G-T

http://identifiers.org/hco/3/GRCh38#108417067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48973684-C-A

108417067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973684-C-G

108417070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973681-A-G

108417095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973660-A-G

108417141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973616-T-C

108421059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973583-C-T

108421108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 48973535-G-A

108421176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 48973467-G-C

108421244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973399-G-A

108421244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973399-G-T

108421248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973397-C-T

108421324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973318-T-A

108421324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973318-T-C

108421507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973168-G-T

108421737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972958-C-T

108421738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972957-C-T

108421811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972885-C-G

108421814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972882-T-C

108422072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972637-C-T

108422557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972466-A-G

108422606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972434-C-G

108436307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48962730-C-T

108439077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48960989-T-A

108439113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48960953-T-C

108439212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48960259-C-G

108439252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48960226-T-G

108439340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48960132-G-A

108439419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48959877-C-G

108439480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48959816-A-G

108439594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48959407-A-G

108439594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48959407-A-T

http://identifiers.org/hco/3/GRCh38#108439598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48959403-C-A

108439598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48959403-C-T

http://identifiers.org/hco/3/GRCh38#108439609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48959392-A-C

108439609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48959392-A-G

108439629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48959372-A-G

108439669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48959333-G-T

108442268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48955514-C-T

108442425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48955366-G-A

108442476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48955314-T-C

108442775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48955018-T-C

108454151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48940300-A-G

108454693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48938861-T-C

108455321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48938130-A-G

108458092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48935766-C-T

108458913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48934856-G-A

108461225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48932597-T-A

http://identifiers.org/hco/3/GRCh38#108462976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48930976-C-A

108462976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48930976-C-T

108462977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48930975-T-C

108462977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48930975-T-G

108463092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48930914-G-T

108463143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: missense variant
orthologous variants: 48930854-C-T

108463266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48930738-G-C

108463305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48930715-A-G

108463732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48930600-C-T

108464216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48930190-G-A

108464323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48930125-C-T

108464489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48929951-T-A

108464489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48929951-T-C

108464492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48929948-A-G

http://identifiers.org/hco/3/GRCh38#108464565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48929874-C-A

108464575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48929864-T-C

108464683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: synonymous variant
orthologous variants: 48929756-C-T

108464702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: missense variant
orthologous variants: 48929737-T-C

108464817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 48929622-G-A

108464836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48929599-A-T

http://identifiers.org/hco/3/GRCh38#108464860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48929577-C-A

108464875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48929562-G-T

108464895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48929542-A-G

108465034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48929440-A-G

108465084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48929409-C-T

108466486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48926396-G-A

108466614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48926266-A-G

108476859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48916497-G-A

http://identifiers.org/hco/3/GRCh38#108476942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48916437-C-A

108476942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48916437-C-T

108482419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48915628-G-A

108482680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48915174-G-A

108483285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48914933-T-C

108483301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48914914-G-C

108483351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48914881-C-G

108483387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48914845-C-T

http://identifiers.org/hco/3/GRCh38#108483417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48914815-A-C

108483417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48914815-A-G

108483452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48914794-G-T

108483609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48914646-A-T

108484205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48914105-C-T

108484955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49156891-T-C

108485055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49156777-T-C

108485173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: synonymous variant
orthologous variants: 49156659-G-T

108485212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: synonymous variant
orthologous variants: 49156620-C-T

108485256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49156572-G-C

108485258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49156570-C-T

108485334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49156477-A-T

108485390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49156410-C-G

108485390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49156410-C-T

http://identifiers.org/hco/3/GRCh38#108485567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49156233-A-C

108485779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49155111-G-C

http://identifiers.org/hco/3/GRCh38#108486012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49154883-A-C

108486014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49154881-G-A

108486094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49154755-T-C

108486200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49154457-C-T

http://identifiers.org/hco/3/GRCh38#108486293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49154133-C-A

108486306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49154123-A-G

http://identifiers.org/hco/3/GRCh38#108486368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49154066-C-A

108486368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49154066-C-G

http://identifiers.org/hco/3/GRCh38#108486415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49154046-A-C

108486415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 49154046-A-G

108486622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49153840-A-G

108486655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49153769-T-C

108486675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49153749-A-G

108486718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49153708-A-T

108486720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49153706-G-T

108486943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49153099-G-C

108486988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49153056-G-C

108487084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49152957-T-C

108487158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 49152883-G-A

108487645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49152406-G-A

108487812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49152296-C-T

108487985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49152115-G-A

108489057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49143449-C-T

108489142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49143364-T-C

108489153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49143353-T-C

http://identifiers.org/hco/3/GRCh38#108489213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49143306-C-A

108489305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49143209-T-A

108489305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49143209-T-G

108489422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49142961-T-C

108489458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49142911-A-T

http://identifiers.org/hco/3/GRCh38#108489533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49142837-A-C

108489556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49142814-G-A

108489556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49142814-G-T

108489994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49142445-C-G

108490414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49141803-C-T

108490468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49141760-C-T

108490855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49141363-G-A

108491439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49141039-G-A

108491588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49139424-G-A

108491613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49139400-A-G

108491750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49139288-G-A

108491750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49139288-G-T

108491762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49139276-C-G

http://identifiers.org/hco/3/GRCh38#108491893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49139157-C-A

108491979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48902208-A-G

108492529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: missense variant
orthologous variants: 48901745-T-G

http://identifiers.org/hco/3/GRCh38#108492634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48901647-A-C

108493173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: missense variant
orthologous variants: 48901536-T-G

108493249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48901487-G-A

108493249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48901487-G-C

108493249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48901487-G-T

http://identifiers.org/hco/3/GRCh38#108493268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48901466-C-A

108493268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48901466-C-G

108493350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48901298-A-G

108493353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48901295-T-A

108493616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48900933-G-A

108494112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48900461-G-A

108494145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48900428-C-G

108494165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48900407-G-A

108494257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48900344-A-G

108494310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48900322-A-G

108494747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48900055-G-A

108494856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48899985-T-A

108495098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49137735-G-A

108495325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49137515-T-C

108495372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49137468-T-C

108495464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49137405-T-C

108495464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49137405-T-G

108495744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49136092-A-T

108495871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 49135972-C-T

http://identifiers.org/hco/3/GRCh38#108495906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49135938-A-C

108495906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49135938-A-G

108495916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49135928-A-G

http://identifiers.org/hco/3/GRCh38#108495997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49135847-C-A

108495997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49135847-C-G

108496077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49135757-A-G

108496690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49127424-G-C

http://identifiers.org/hco/3/GRCh38#108496770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49127358-C-A

108497222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49127250-T-A

108497446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49127032-A-G

108497601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49126798-G-A

108497601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49126798-G-T

108497802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49126250-C-T

108497915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49126110-A-G

http://identifiers.org/hco/3/GRCh38#108497989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49126032-A-C

http://identifiers.org/hco/3/GRCh38#108497994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49126027-C-A

http://identifiers.org/hco/3/GRCh38#108498023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49125999-C-A

108498023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49125999-C-G

108498035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49125987-G-T

http://identifiers.org/hco/3/GRCh38#108498036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49125986-C-A

108498036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49125986-C-G

108498087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: missense variant
orthologous variants: 49125935-T-C

108498207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49125818-G-C

108498207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49125818-G-T

108498209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49125816-T-C

108498508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49125809-A-T

108498671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49125689-C-T

108499347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49125034-A-G

108499527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49124867-T-C

108499527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49124867-T-G

108499640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49124755-A-G

108499900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49124501-T-C

108499900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49124501-T-G

108500117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: splice donor variant
orthologous variants: 49124286-C-T

108500209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: synonymous variant
orthologous variants: 49124194-T-C

108500270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: missense variant
orthologous variants: 49124133-T-C

http://identifiers.org/hco/3/GRCh38#108500319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49124084-C-A

108500390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49124014-G-A

108500390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49124014-G-C

108500390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49124014-G-T

http://identifiers.org/hco/3/GRCh38#108500395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49124007-C-A

108500395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49124007-C-T

http://identifiers.org/hco/3/GRCh38#108500542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49123857-C-A

108501552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48885604-T-C

108501680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48885498-A-T

108501734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: missense variant
orthologous variants: 48885438-C-T

108501829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: synonymous variant
orthologous variants: 48885343-G-T

108501877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48885295-A-G

108502812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49123325-T-C

108502834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49123294-C-T

108503064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49123100-T-C

108503111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49123050-T-C

108503270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49122872-G-A

108503464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49122670-G-A

108504268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49112993-T-C

108504400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49112874-T-C

108504400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49112874-T-G

108504582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49112720-C-G

108505601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48882070-T-A

108505601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48882070-T-C

108505645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48882029-A-G

108505663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48882012-A-G

108505683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48881987-G-A

108505683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48881987-G-T

108505715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 48881957-T-C

108505715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 48881957-T-G

108505892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48881790-A-G

108505949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48881739-G-A

108506063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48881624-T-C

108506512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48881210-A-G

108506544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48881164-T-C

108507472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48880956-T-C

108508059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48880321-C-T

108508070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48880310-T-G

108508309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48880079-T-C

http://identifiers.org/hco/3/GRCh38#108508312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48880076-C-A

108508403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48879978-A-G

108508404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48879977-T-C

108508436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48879945-C-T

108508796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48879582-T-G

108509119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48879255-C-T

108509511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48878854-G-A

108509625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48878736-T-C

108509647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48878718-C-T

108509686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48878678-A-G

108509692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48878672-T-C

108509963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48878394-A-G

108509985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48878374-C-T

http://identifiers.org/hco/3/GRCh38#108510265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48878105-C-A

108510296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48878074-A-G

108510296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48878074-A-T

108510342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48878030-T-C

http://identifiers.org/hco/3/GRCh38#108510383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48877989-C-A

108510383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48877989-C-T

108510450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: synonymous variant
orthologous variants: 48877924-G-A

108510583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 48877775-T-A

108510583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 48877775-T-C

108510680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48877693-T-A

108510680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48877693-T-G

108510771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48877639-A-T

108511100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48877310-A-T

http://identifiers.org/hco/3/GRCh38#108511153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48877264-C-A

108511391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48877037-G-A

108511391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48877037-G-T

108512318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49106911-T-G

108512384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49106842-T-C

108513265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49105140-G-A

http://identifiers.org/hco/3/GRCh38#108513436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49105034-C-A

http://identifiers.org/hco/3/GRCh38#108513505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49104984-A-C

108513513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49104976-C-T

108513603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49104880-T-C

108514611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48876907-G-A

108514611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48876907-G-C

108514954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48876587-C-T

http://identifiers.org/hco/3/GRCh38#108515026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48876536-C-A

108515225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48876350-G-A

108515308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48876269-T-C

http://identifiers.org/hco/3/GRCh38#108515377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48876203-C-A

http://identifiers.org/hco/3/GRCh38#108515521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48876082-C-A

108515718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48875679-T-C

108516000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48875052-T-A

108516234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48874839-T-A

108516722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48874362-T-C

108516787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48874298-G-T

108516882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49099225-T-C

108516962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49099130-T-A

108516962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49099130-T-C

108516990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49099111-G-A

108517343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48872470-T-G

108519601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48870783-G-A

108519638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48870746-A-G

http://identifiers.org/hco/3/GRCh38#108519689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48870697-C-A

http://identifiers.org/hco/3/GRCh38#108519939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48870468-A-C

108520137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48870267-A-G

108520165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48870237-A-G

http://identifiers.org/hco/3/GRCh38#108520557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#48869863-A-C

108520997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48869459-G-A

108520997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48869459-G-T

108521280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48868937-A-G

108521697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48868517-G-A

108521734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48868497-A-G

108522052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48868182-T-C

108522969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49093710-C-T

108523126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49093569-A-G

108523152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49093543-A-G

108523301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49093369-T-A

108523568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48867625-T-C

108523582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48867611-G-C

108523583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48867610-G-A

108523626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 48867572-G-T

108523819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49093004-G-A

http://identifiers.org/hco/3/GRCh38#108523917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#49092923-A-C

108523929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49092883-A-T

108524049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49092764-T-C

108524063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49092750-T-G

108524224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49092585-T-C

108524224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49092585-T-G

108524226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49092568-T-C

108524227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49092567-A-G

108524239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49092551-C-T

108524243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49092547-C-G

108524324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49092469-A-T

108524341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron variant
orthologous variants: 49092451-T-C

108525165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48865005-T-C

108525252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48864881-T-C

108525257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48864876-T-A

108525270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48864842-T-C

108525297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48864782-G-T

108525389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48864719-T-A

108525395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48864713-G-A

108525477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48864608-G-C

108525737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48864333-G-C

108525750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48864322-T-C

108525799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48864278-G-A

108525945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48864001-T-A

108525945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48864001-T-C

108526046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48863887-A-G

108526560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48863290-G-A

108526560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48863290-G-T

108527277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48862850-T-C

108527278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31073
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 48862849-T-C