28958124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71969498-G-A

28958163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71969537-T-G

28958630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71969668-A-G

28958838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71969838-C-G

28958838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71969838-C-T

28958840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71969840-C-T

28958842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71969842-G-A

28966825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71970766-A-G

28966825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71970766-A-T

28966907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71970829-C-T

28970781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71973383-G-A

28970820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71973422-A-G

28970868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71973470-G-T

28970923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71973525-G-A

28970923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71973525-G-T

http://identifiers.org/hco/2/GRCh38#28970946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71973545-C-A

28970979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71973578-A-G

28970982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71973581-G-A

28970982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71973581-G-T

28970995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71973649-T-A

28970995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71973649-T-C

28971055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71973688-T-A

28971055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71973688-T-C

http://identifiers.org/hco/2/GRCh38#28971096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71973725-C-A

28971146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71973768-T-C

28971178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71973799-T-C

28971786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71974060-A-T

28971818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71974095-G-A

28971844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71974120-G-A

28971893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71974168-A-T

28971894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71974169-G-C

28972066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71974348-A-G

28972074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71974356-A-G

28972637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71974424-A-G

28972663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71974450-G-A

28976935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71977187-C-T

http://identifiers.org/hco/2/GRCh38#28977173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71977379-C-A

28977173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71977379-C-T

28977260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71977468-A-G

28977405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71977574-C-G

28977582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71977725-C-T

28977583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71977726-G-A

28977692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71977815-C-T

28977752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71977855-G-C

28977764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71977867-G-A

28977764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71977867-G-C

28978258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71977926-G-T

28978331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71977986-A-G

28980346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71979356-T-C

28980478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71979501-C-T

28980728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71979690-T-C

28981002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71979913-G-C

28981027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71979940-A-T

28981201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron variant
orthologous variants: 71980130-C-T

28981238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, undefined
orthologous variants: 71980198-G-A

28981238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, undefined
orthologous variants: 71980198-G-T

28981325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71980283-G-T

28981344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 71980302-G-A

28981344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 71980302-G-T

28981387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71980343-G-A

http://identifiers.org/hco/2/GRCh38#28981424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71980381-C-A

http://identifiers.org/hco/2/GRCh38#28981476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71980432-C-A

28981552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71980513-G-A

28981552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71980513-G-T

28981768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71980677-C-T

28981986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71980864-G-T

28982089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71980966-A-G

28982135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71980997-A-G

28982173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71981027-C-T

28982215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71981064-G-A

28982215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71981064-G-T

28982662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71981589-C-G

28982672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71981599-C-T

28982673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71981600-G-A

28982720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71981647-C-T

28982852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71981723-G-A

28983485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71981973-G-C

28983747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71982263-G-T

28983791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71982304-C-T

28983976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71982446-T-C

28984192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71982643-A-G

28984239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71982693-G-A

28984943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71983347-T-C

http://identifiers.org/hco/2/GRCh38#28984950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71983354-C-A

28985024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71983419-G-A

http://identifiers.org/hco/2/GRCh38#28985050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71983445-C-A

28985211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71983600-T-A

28985215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71983604-A-G

http://identifiers.org/hco/2/GRCh38#28985242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71983631-C-A

28985408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71983738-C-T

28985424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71983754-A-G

28986402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71985068-G-T

28986425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71985091-G-A

28986425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71985091-G-C

28986425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71985091-G-T

28986580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71985257-T-C

28986767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71985439-A-G

28987113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71987065-A-G

28987447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71987381-G-A

28987684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71987646-T-C

28987802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71987764-A-G

28991698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71989599-G-A

28991703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71989604-G-A

28992031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71989906-G-C

28992123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71989994-G-T

28992184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71990037-G-C

http://identifiers.org/hco/2/GRCh38#28992492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71990347-C-A

http://identifiers.org/hco/2/GRCh38#28992678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71990521-C-A

28992678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71990521-C-G

28993540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71991011-G-A

28993748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71991150-G-A

28993789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71991191-G-A

28993795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71991197-C-T

28993840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71991242-T-C

28994027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71991392-C-T

28994191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71991576-G-T

28994292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71991667-C-T

28994462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71991807-G-A

28994462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71991807-G-C

28994533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71991878-C-T

28994597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71991941-G-A

28994597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71991941-G-T

http://identifiers.org/hco/2/GRCh38#28994656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71991998-C-A

28994664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71992006-G-T

28994688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71992025-G-T

28994734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71992059-G-A

28994734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 71992059-G-T

28994846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71992171-T-C

28994850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71992175-G-A

28994850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71992175-G-C

28994850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71992175-G-T

28994954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71992231-G-A

28994963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71992240-G-A

28994963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71992240-G-T

28994967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71992244-T-C

28994968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71992245-G-A

28994968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71992245-G-T

28995087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71992359-G-A

http://identifiers.org/hco/2/GRCh38#28995796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71993146-C-A

28995905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71993290-G-A

28997397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71993815-T-G

28997614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71994028-G-C

28997614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71994028-G-T

28997997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71994462-G-T

28998045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71994491-G-A

28998045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71994491-G-T

28998064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71994506-G-A

28998064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71994506-G-T

http://identifiers.org/hco/2/GRCh38#28998159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71994597-C-A

28998159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71994597-C-T

28998246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71994687-T-C

28999244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71996207-G-T

http://identifiers.org/hco/2/GRCh38#28999311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71996274-C-A

28999311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71996274-C-T

28999343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71996306-A-T

28999347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71996310-G-A

28999455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71996418-A-G

http://identifiers.org/hco/2/GRCh38#28999487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71996440-C-A

28999487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71996440-C-T

28999494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71996447-T-A

28999494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71996447-T-C

http://identifiers.org/hco/2/GRCh38#28999521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71996474-C-A

28999521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71996474-C-G

28999521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71996474-C-T

28999560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71996514-G-T

28999583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71996533-G-A

28999583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71996533-G-C

29002279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71997256-T-C

29002296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71997269-C-G

29002392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71997363-G-A

29002392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71997363-G-T

29002399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71997380-T-C

29002399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71997380-T-G

http://identifiers.org/hco/2/GRCh38#29002414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71997395-A-C

29002414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71997395-A-G

http://identifiers.org/hco/2/GRCh38#29002448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71997436-C-A

http://identifiers.org/hco/2/GRCh38#29002470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71997455-C-A

29002470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71997455-C-T

29002475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71997460-T-A

http://identifiers.org/hco/2/GRCh38#29002479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71997464-C-A

29002554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71997539-G-T

29002678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71997663-C-G

http://identifiers.org/hco/2/GRCh38#29002826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71997765-C-A

29002826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71997765-C-T

http://identifiers.org/hco/2/GRCh38#29002839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71997778-C-A

29002839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71997778-C-G

29002989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71997925-G-A

29003130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71998068-C-T

29003210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71998105-A-G

29003319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71998232-G-C

29003343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71998256-T-A

29003343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71998256-T-C

29003343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71998256-T-G

http://identifiers.org/hco/2/GRCh38#29003375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71998288-C-A

http://identifiers.org/hco/2/GRCh38#29003388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71998306-C-A

29003388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71998306-C-G

29003388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71998306-C-T

29003515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71998464-G-A

29003515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71998464-G-T

29003725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71998697-T-A

29003725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71998697-T-C

http://identifiers.org/hco/2/GRCh38#29003730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71998702-C-A

29003730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71998702-C-T

29003757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71998724-T-C

http://identifiers.org/hco/2/GRCh38#29003769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71998736-C-A

29003769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71998736-C-T

29003789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71998754-G-T

http://identifiers.org/hco/2/GRCh38#29003820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#71998785-C-A

29006700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71999905-G-T

29006762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71999965-C-G

29006762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71999965-C-T

29006818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72000004-C-T

29006853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72000024-C-T

http://identifiers.org/hco/2/GRCh38#29006859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72000030-C-A

29006859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72000030-C-T

29006901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72000059-C-T

29006912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72000070-C-T

29007087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72000219-G-A

29007087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72000219-G-C

29007284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72000394-C-T

29007372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72000454-G-A

http://identifiers.org/hco/2/GRCh38#29007790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72000888-C-A

29007832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72000935-C-G

29007916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72001002-C-T

http://identifiers.org/hco/2/GRCh38#29007920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72001006-A-C

29008001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72001129-G-C

29008001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72001129-G-T

29008844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72001356-T-G

29008853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72001365-G-C

29008968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72001478-G-A

http://identifiers.org/hco/2/GRCh38#29009203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72001737-A-C

29009209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72001743-G-A

29011287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72002569-C-G

29011308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72002587-G-A

29011308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72002587-G-T

29011354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72002611-A-G

29011354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72002611-A-T

29011372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72002624-T-C

http://identifiers.org/hco/2/GRCh38#29011405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72002649-C-A

http://identifiers.org/hco/2/GRCh38#29011430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72002669-C-A

29011430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72002669-C-T

29011499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 72002736-T-C

http://identifiers.org/hco/2/GRCh38#29011551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72002785-C-A

29011551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72002785-C-T

29011663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72002888-G-T

29011773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72002994-C-T

http://identifiers.org/hco/2/GRCh38#29011777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72002998-A-C

29011945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72003168-C-T

29012235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72003493-G-T

29012238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72003496-G-A

29012315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72003560-G-T

29012443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72003683-G-C

29012853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72004002-G-T

29013000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72004092-G-A

http://identifiers.org/hco/2/GRCh38#29013041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72004110-C-A

29013047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72004116-C-T

29013090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72004159-C-T

29014300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72004726-T-A

29014396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 72004829-G-A

29014416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72004849-C-T

http://identifiers.org/hco/2/GRCh38#29014423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72004856-A-C

http://identifiers.org/hco/2/GRCh38#29014476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72004909-C-A

29014476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72004909-C-T

29014518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72004948-G-A

29014518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72004948-G-T

29014583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005013-G-A

29014583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005013-G-T

http://identifiers.org/hco/2/GRCh38#29014629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72005048-A-C

29014629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005048-A-T

http://identifiers.org/hco/2/GRCh38#29014634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72005053-C-A

29014634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005053-C-G

29014651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005069-G-A

29014651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005069-G-T

29014652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005075-G-T

http://identifiers.org/hco/2/GRCh38#29014681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72005116-C-A

29014681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005116-C-G

29014681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005116-C-T

29014708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005144-G-A

29014708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005144-G-T

http://identifiers.org/hco/2/GRCh38#29014709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72005145-C-A

29014709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005145-C-T

http://identifiers.org/hco/2/GRCh38#29014710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72005146-C-A

29014710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005146-C-G

29014710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005146-C-T

29014920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005332-T-C

29014920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005332-T-G

29015198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005608-T-G

29015324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005713-G-A

29015363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72005755-T-C

29015744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72006001-T-G

29015781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72006037-G-T

29015842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72006090-C-G

29015902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72006146-A-G

29015911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72006155-C-T

29016275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72006489-C-G

http://identifiers.org/hco/2/GRCh38#29016378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72006649-C-A

29016378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72006649-C-G

29016378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72006649-C-T

29016448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72006771-A-G

29016490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72006823-T-C

29016638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72006985-G-A

29016723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72007064-A-G

29016982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72007306-G-T

29017022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72007350-G-A

29017108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72007441-T-C

29017108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72007441-T-G

29017263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72007609-C-G

29017283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 72007629-C-T

http://identifiers.org/hco/2/GRCh38#29017786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72007869-C-A

29017810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72007893-G-A

http://identifiers.org/hco/2/GRCh38#29017821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72007904-C-A

29017851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72007934-T-C

29017868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72007951-C-T

http://identifiers.org/hco/2/GRCh38#29017997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72008059-C-A

29017997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72008059-C-G

29017997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72008059-C-T

http://identifiers.org/hco/2/GRCh38#29018053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72008107-C-A

29018062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72008116-G-T

29018179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72008145-G-C

29018275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72008226-T-G

http://identifiers.org/hco/2/GRCh38#29018324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72008259-C-A

29018324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72008259-C-T

http://identifiers.org/hco/2/GRCh38#29018357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72008290-C-A

29018357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72008290-C-T

29018383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72008309-G-A

29018383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72008309-G-C

29018462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72008385-T-G

http://identifiers.org/hco/2/GRCh38#29018473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72008399-C-A

29018476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72008402-A-T

29018477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72008403-T-A

29018477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72008403-T-C

29018498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72008424-G-T

http://identifiers.org/hco/2/GRCh38#29018655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72008582-C-A

29018655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72008582-C-T

29018656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72008583-T-C

29022105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72011636-G-A

29022105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72011636-G-C

29022105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72011636-G-T

29022109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72011640-T-C

29022114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72011645-T-C

29022116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72011647-T-C

http://identifiers.org/hco/2/GRCh38#29022117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72011648-C-A

http://identifiers.org/hco/2/GRCh38#29022194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72011719-C-A

29022261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72011789-G-A

29022261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72011789-G-C

http://identifiers.org/hco/2/GRCh38#29022345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72011875-C-A

29022345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72011875-C-T

29022483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72012000-C-T

29022484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72012001-G-A

29022488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72012005-G-A

29022681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72012445-T-C

29022708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72012477-G-A

29022799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72012562-G-T

29022954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72012681-G-T

http://identifiers.org/hco/2/GRCh38#29022967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72012694-C-A

29022967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72012694-C-T

29023217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72012908-T-C

http://identifiers.org/hco/2/GRCh38#29023219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72012910-C-A

29023219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72012910-C-T

29023273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72012976-T-C

29023317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013017-C-T

http://identifiers.org/hco/2/GRCh38#29023321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72013021-C-A

29023321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013021-C-T

29023322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013022-A-G

29023322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013022-A-T

29023323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013023-C-T

29023501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013201-A-G

29023642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013328-G-T

29023692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013379-G-A

http://identifiers.org/hco/2/GRCh38#29023694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72013381-C-A

29023705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013397-G-A

29023777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013526-T-C

29023997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013931-G-A

29023997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013931-G-T

http://identifiers.org/hco/2/GRCh38#29024008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72013946-C-A

29024008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013946-C-T

29024042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013981-G-A

29024042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013981-G-C

29024042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013981-G-T

29024043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013982-G-A

29024043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013982-G-C

29024043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013982-G-T

29024055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013999-G-A

29024055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72013999-G-T

29024056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014000-G-A

29024056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014000-G-T

29024065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014009-G-A

29024065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014009-G-T

http://identifiers.org/hco/2/GRCh38#29024071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72014015-A-C

http://identifiers.org/hco/2/GRCh38#29024092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72014024-C-A

29024092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014024-C-T

29024117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014050-G-A

29024119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014052-G-A

29024119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014052-G-T

29024133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72014066-T-C

http://identifiers.org/hco/2/GRCh38#29024167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72014102-A-C

29024167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72014102-A-T

29024184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72014119-T-A

29024184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72014119-T-C

http://identifiers.org/hco/2/GRCh38#29024203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72014138-C-A

29024244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72014179-C-T

29024285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72014220-C-T

29024410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72014425-T-G

29024420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 72014435-T-G

29024429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014443-G-A

29024429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014443-G-T

29024433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014447-G-A

29024433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014447-G-T

29024438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014452-C-T

29024446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014460-G-A

29024446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014460-G-T

http://identifiers.org/hco/2/GRCh38#29024523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72014541-C-A

29024523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014541-C-T

29024550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014591-T-A

http://identifiers.org/hco/2/GRCh38#29024552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72014593-C-A

29024725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72014883-C-T

http://identifiers.org/hco/2/GRCh38#29025063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72015175-C-A

29025109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015219-G-A

29025139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015248-C-T

29025179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015288-T-C

29025180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015289-T-C

29025183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015292-C-T

29025270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015351-T-A

29025273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015354-G-A

29025395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015466-T-A

29025406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015477-G-T

29025430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015503-C-T

29025589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015677-A-G

29025655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015743-C-T

29025675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015774-G-A

29025767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015869-C-G

29025767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015869-C-T

29026367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72015998-C-T

http://identifiers.org/hco/2/GRCh38#29026392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72016041-C-A

29026561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016197-G-A

29026603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016239-C-G

29026603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016239-C-T

29026672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016318-G-A

29026685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016331-G-C

29026685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016331-G-T

http://identifiers.org/hco/2/GRCh38#29026719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72016365-C-A

29026719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016365-C-T

29026720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016366-A-G

29026739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016380-G-A

29026739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016380-G-T

http://identifiers.org/hco/2/GRCh38#29026742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72016383-C-A

29026742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016383-C-T

29026769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016416-G-A

29026769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016416-G-T

29026776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016423-T-A

29026776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016423-T-C

29026787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016436-T-G

http://identifiers.org/hco/2/GRCh38#29026790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72016439-C-A

29026790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016439-C-T

http://identifiers.org/hco/2/GRCh38#29026794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72016443-C-A

29026794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016443-C-T

29026834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016482-G-T

http://identifiers.org/hco/2/GRCh38#29026836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72016484-C-A

29026836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016484-C-T

http://identifiers.org/hco/2/GRCh38#29026837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72016485-C-A

29026837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016485-C-T

29026883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72016534-G-A

29026883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72016534-G-C

29026883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72016534-G-T

http://identifiers.org/hco/2/GRCh38#29026919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72016570-C-A

29026919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72016570-C-T

29026922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72016573-T-C

29026938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72016589-G-A

29026938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72016589-G-T

29027019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72016670-A-G

http://identifiers.org/hco/2/GRCh38#29027050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72016700-C-A

29027050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016700-C-T

http://identifiers.org/hco/2/GRCh38#29027116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72016759-C-A

29027169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016811-T-G

29027257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72016911-T-C

29030591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72018363-A-G

29030831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72018935-C-T

29030839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72018943-G-A

29030848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72018952-T-A

29030941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72019045-T-G

29031662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72019574-A-G

29031769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72019658-C-T

29032030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72019899-C-T

29032150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72020147-T-C

29032198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72020194-T-C

29032284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72020259-C-T

29032287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 72020262-G-T

29032414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72020349-G-A

29032434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72020369-C-T

29032470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72020406-C-T

29032484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72020420-C-T

29032485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72020421-G-A

29032624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72020924-T-A

29032701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72020996-A-G

29032744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 72021039-T-C

http://identifiers.org/hco/2/GRCh38#29033000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72021297-A-C

29033000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72021297-A-G

29033042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72021339-T-G

29033150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72021412-A-G

29033150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72021412-A-T

http://identifiers.org/hco/2/GRCh38#29033153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72021415-C-A

29033153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72021415-C-T

http://identifiers.org/hco/2/GRCh38#29033282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#72021511-C-A

http://identifiers.org/hco/2/GRCh38#29033351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#72021571-A-C

29033351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72021571-A-T

http://identifiers.org/hco/2/GRCh38#29033448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#72021653-C-A

29033558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 72021762-G-A

29033615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72021817-G-A

29033818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72021993-G-A

29033947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72022114-A-G

29034177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72022314-C-T

29034654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72022721-A-T

29034715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72022777-G-A

29034973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72022976-A-G

http://identifiers.org/hco/2/GRCh38#29035141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72022992-A-C

29035141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72022992-A-G

29035408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023267-G-C

29035408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023267-G-T

29035457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72023310-T-C

29035528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72023384-G-A

29035528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72023384-G-T

http://identifiers.org/hco/2/GRCh38#29035540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72023396-C-A

29035540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72023396-C-T

29035594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72023450-G-A

29035594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72023450-G-C

29035594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72023450-G-T

29035636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72023492-G-A

29035636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72023492-G-C

29035636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72023492-G-T

29035668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023519-T-C

29035669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023520-T-G

29035670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023521-G-A

29035670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023521-G-C

29035670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023521-G-T

29035672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023523-T-C

29035672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023523-T-G

29035678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023529-T-A

29035678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023529-T-C

29035718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023571-T-C

http://identifiers.org/hco/2/GRCh38#29035772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72023625-C-A

29035772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023625-C-T

29035911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023723-G-T

29035952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023765-T-A

29035992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72023804-A-G

29036392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72024133-T-G

29036393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72024134-T-G

29036519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72024219-T-G

29036533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72024237-T-C

29036606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72024310-G-T

29036810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72024540-G-C

29036842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72024618-G-A

29036842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72024618-G-T

29036853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72024659-G-T

29036889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72024703-G-T

29036904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72024761-T-C

29036904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72024761-T-G

29036923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72024782-G-A

http://identifiers.org/hco/2/GRCh38#29037219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72025166-C-A

29037219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72025166-C-G

29037258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72025211-C-T

29037283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72025237-A-G

29037394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72025338-G-C

29037556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72025437-C-T

http://identifiers.org/hco/2/GRCh38#29037632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72025501-C-A

29037751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72025624-C-T

29038064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72025938-G-A

29038064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72025938-G-T

29038159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72026027-G-C

29038244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72026859-C-T

29038362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72026998-G-A

29038804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72027177-C-T

29038805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72027178-T-C

29038940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72027282-G-C

29039297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72027557-G-C

29039504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72027764-T-G

29039519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72027779-G-A

29039572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72027834-G-T

29039782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72028039-T-C

29039986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72028244-G-A

29041715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72029348-C-T

29042233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72029986-C-T

29042264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72030048-T-C

29042367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72030180-A-G

http://identifiers.org/hco/2/GRCh38#29043645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72030679-A-C

29044660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031002-C-G

29044678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031018-A-G

29044720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031059-T-C

29044778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031118-C-T

29044882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031221-G-C

http://identifiers.org/hco/2/GRCh38#29045016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72031313-A-C

29045073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031358-A-G

29045092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031374-A-G

29045109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031392-G-T

http://identifiers.org/hco/2/GRCh38#29045206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72031851-C-A

http://identifiers.org/hco/2/GRCh38#29045213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72031858-C-A

http://identifiers.org/hco/2/GRCh38#29045214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72031859-C-A

29045214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031859-C-G

29045214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031859-C-T

29045232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031877-T-A

http://identifiers.org/hco/2/GRCh38#29045254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72031898-C-A

29045254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031898-C-T

29045258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031902-G-A

29045258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031902-G-T

http://identifiers.org/hco/2/GRCh38#29045263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72031907-C-A

http://identifiers.org/hco/2/GRCh38#29045264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72031908-C-A

29045264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031908-C-G

29045264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031908-C-T

29045303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72031947-G-T

29045355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72031998-G-A

29045355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72031998-G-C

29045382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72032025-G-A

http://identifiers.org/hco/2/GRCh38#29045428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72032071-C-A

29045428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72032071-C-T

http://identifiers.org/hco/2/GRCh38#29045430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72032073-C-A

29045430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72032073-C-T

http://identifiers.org/hco/2/GRCh38#29045448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72032091-C-A

29045448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72032091-C-G

29045448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72032091-C-T

29045506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72032133-G-A

http://identifiers.org/hco/2/GRCh38#29045568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72032182-C-A

http://identifiers.org/hco/2/GRCh38#29045577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72032191-C-A

29046915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72033368-G-A

29046915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72033368-G-T

29046926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72033386-T-C

29046963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72033432-G-A

29046963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 72033432-G-T

29047020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72033486-A-G

http://identifiers.org/hco/2/GRCh38#29047041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72033510-C-A

29047041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72033510-C-T

http://identifiers.org/hco/2/GRCh38#29047124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72033592-C-A

29049914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72034360-G-A

29050254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72034487-A-G

29050255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72034488-G-A

29050255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72034488-G-T

29050406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72034505-T-C

29050742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72034812-G-T

http://identifiers.org/hco/2/GRCh38#29050748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72034818-C-A

29050748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72034818-C-T

29050819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72034849-T-C

http://identifiers.org/hco/2/GRCh38#29050861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72034881-C-A

29050861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72034881-C-T

http://identifiers.org/hco/2/GRCh38#29050862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72034882-A-C

29050965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72034951-A-G

29051072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72035065-G-T

http://identifiers.org/hco/2/GRCh38#29051115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72035107-C-A

29051185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72035645-C-T

29051210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72035670-A-G

29051229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72035689-T-C

29051263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72035718-T-G

29051274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72035732-G-A

29051274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72035732-G-T

29051287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72035745-T-C

29051375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72035832-A-G

29051547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72035988-A-G

29051582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72036008-T-C

http://identifiers.org/hco/2/GRCh38#29051652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72036078-C-A

29051652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72036078-C-T

29051653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72036079-T-C

29051673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72036113-G-A

29051673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72036113-G-T

29051805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72036232-T-C

http://identifiers.org/hco/2/GRCh38#29051814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72036241-C-A

29051814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72036241-C-T

http://identifiers.org/hco/2/GRCh38#29051845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72036272-A-C

29051845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72036272-A-G

29051845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72036272-A-T

29052051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 72036478-C-G

29052051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72036478-C-T

29052078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 72036505-T-C

29052096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 72036523-A-G

http://identifiers.org/hco/2/GRCh38#29052166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33715
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#72036602-C-A