http://identifiers.org/hco/6/GRCh38#168441227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14499838-C-A

168441227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 5 prime UTR variant
orthologous variants: 14499838-C-T

168441260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 14499871-G-A

168441260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 14499871-G-C

http://identifiers.org/hco/6/GRCh38#168441264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#14499875-C-A

168441264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 14499875-C-T

http://identifiers.org/hco/6/GRCh38#168441276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#14499889-C-A

168441276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 14499889-C-T

http://identifiers.org/hco/6/GRCh38#168441280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#14499893-C-A

168441280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 14499893-C-T

168441302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 14499909-G-A

168441302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 14499909-G-T

168441336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 5 prime UTR variant
orthologous variants: 14499939-G-A

168441336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 5 prime UTR variant
orthologous variants: 14499939-G-C

168441336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 5 prime UTR variant
orthologous variants: 14499939-G-T

168441533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, undefined
orthologous variants: 14500122-G-A

168441533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, undefined
orthologous variants: 14500122-G-C

168441533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, undefined
orthologous variants: 14500122-G-T

168441587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14500156-G-A

168441587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14500156-G-T

168441625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, undefined
orthologous variants: 14500191-A-G

168442015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14500487-G-A

168442166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14500664-A-G

168442226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14500718-G-T

168442332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14500824-C-T

168442422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14500912-G-A

168442422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14500912-G-T

168442572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14501059-G-C

168442765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14501219-A-G

168443801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14502251-G-A

168443908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14502373-T-A

168443908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14502373-T-C

168443908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14502373-T-G

168444059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14502477-T-C

168444082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14502500-G-A

168444243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14502607-C-T

http://identifiers.org/hco/6/GRCh38#168446388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14503374-A-C

168446388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14503374-A-G

168446395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14503381-T-G

168446531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14503513-G-C

168446978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: -G-A

168447015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: -C-G

168447143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: -T-C

168447733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: -C-T

168447809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14504447-A-G

168447821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14504459-G-T

168447872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14504508-G-T

168448204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14504817-A-G

168449429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14505770-A-G

168449442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14505783-T-C

168449524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14505855-G-C

168449607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14505933-T-C

168450165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14507106-A-G

168450313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14507253-A-T

168450614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14507516-G-C

168450621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14507523-G-A

168450621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14507523-G-T

168450706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14507569-G-C

168450736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14507592-A-T

168450952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14507787-T-A

168451035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14507867-G-C

168451058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14507887-C-T

168451095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14507922-T-C

168451396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14508157-G-A

168451413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14508173-G-A

168451536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14508279-C-T

168451593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14508316-G-C

168452372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14508962-G-T

168457472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14511171-C-T

168457494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14511194-A-G

168457553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14511255-G-A

168459385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14515560-G-A

168460114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14515919-A-T

168460138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14515930-G-A

168460357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14516135-G-A

168460449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14516227-C-T

168460476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14516252-G-T

168460711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14516494-C-T

168466437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14520475-G-A

168466643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14520669-G-T

168466685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14520710-G-A

168467812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: -G-A

168467812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: -G-T

168469343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14522516-G-C

168469401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14522581-G-C

168469522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14522701-A-G

168469530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14522709-A-T

168469562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14522739-C-T

168469572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14522749-T-C

168469583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14522760-A-G

168469583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14522760-A-T

http://identifiers.org/hco/6/GRCh38#168469594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14522771-A-C

168469769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14522923-G-T

168469821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14522964-C-T

168470840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14523693-A-G

168471984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14525534-C-G

168472146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14525688-T-G

168472427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14525956-T-C

168472488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14525991-A-T

168472558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14526007-A-G

168472625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14526067-G-A

168472650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14526096-T-C

168473080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14526509-G-T

168476470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14528871-G-A

168476931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14529403-T-C

168476963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14529435-A-G

http://identifiers.org/hco/6/GRCh38#168477132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14529603-C-A

168477232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14529679-G-C

168477360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14529774-A-G

168477379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14529787-G-C

168477379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14529787-G-T

168477499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14529863-C-T

http://identifiers.org/hco/6/GRCh38#168479438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14530592-A-C

168479438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14530592-A-G

168479621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14530845-C-T

168479676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14530906-G-T

168479979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14531203-G-A

168480003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14531240-G-T

168480239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14531402-G-A

168480518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14531654-T-C

168480534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14531672-C-T

168486513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14532169-A-G

http://identifiers.org/hco/6/GRCh38#168492400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14533673-C-A

168492595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14533900-T-C

168492811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14534098-G-A

168493484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14534221-A-T

168493526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14534262-C-T

168493575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14534299-C-G

168493628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14534352-A-G

168493631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14534357-G-A

168493767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14534489-T-A

168493816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14534522-A-G

168493821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14534527-A-G

168494137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14534831-T-G

168495980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14537156-C-T

168495981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14537157-G-A

168496093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14537259-T-C

168496170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14537340-G-T

168496412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14537574-A-G

168496454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14537617-C-T

168496579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14537738-G-A

168496846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14538000-T-C

168496856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14538014-A-G

168498110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14539863-G-A

168498256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14539998-T-G

168498322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14540064-G-A

168501002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14541972-G-T

168501011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14541981-C-T

168501162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14542115-T-C

168501253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14542180-T-G

168501291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14542218-T-C

168501293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14542220-A-G

168501482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14542392-G-A

168501482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14542392-G-T

168501567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14542488-G-A

168501747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14542596-C-G

168501759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14542608-G-T

168501811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14542657-G-A

168501811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14542657-G-T

168501812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14542658-T-C

168501812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14542658-T-G

168501935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14542760-C-G

168501946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14542772-G-A

168502234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14543056-C-T

168502292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14543112-C-T

168502301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14543121-T-C

168502422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14543224-C-T

http://identifiers.org/hco/6/GRCh38#168509773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14545677-C-A

168509773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14545677-C-T

168509809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14545713-A-G

http://identifiers.org/hco/6/GRCh38#168509894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14545778-C-A

168509926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: synonymous variant
orthologous variants: 14545808-G-A

168509998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: synonymous variant
orthologous variants: 14545880-C-T

168510117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14545997-A-G

168510123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14546003-A-G

168510140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14546020-G-A

168510159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14546036-T-A

168510229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14546095-A-G

http://identifiers.org/hco/6/GRCh38#168510390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14546460-C-A

168513341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14547515-G-A

168513405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14547607-C-T

168513460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14547673-C-T

168513520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14547755-C-T

http://identifiers.org/hco/6/GRCh38#168514827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14548532-C-A

168514827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14548532-C-G

168514872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14548583-A-T

168514877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14548588-G-A

168515123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14548797-A-G

168515163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14548835-A-G

168515232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14548894-G-A

168515401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14549059-T-C

168515457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14549109-C-G

168515496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14549137-T-G

168515588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, undefined
orthologous variants: 14549165-C-T

http://identifiers.org/hco/6/GRCh38#168515688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#14549243-A-C

168515693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, undefined
orthologous variants: 14549248-T-A

168515693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, undefined
orthologous variants: 14549248-T-C

168515890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14549418-C-T

168516177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14549675-A-G

168516232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14549729-G-A

168519004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14550775-T-G

http://identifiers.org/hco/6/GRCh38#168519009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14550780-A-C

168519009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14550780-A-G

168519054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14550833-T-C

168519061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14550840-G-A

http://identifiers.org/hco/6/GRCh38#168519092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14550879-A-C

168519425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551033-A-G

168519591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551163-A-G

168519652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551218-G-A

168519708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551265-G-A

168519760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551315-A-G

168519763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551318-C-G

http://identifiers.org/hco/6/GRCh38#168519778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14551333-C-A

168519822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551380-C-T

168519832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551390-T-G

168519838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551396-A-G

168519838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551396-A-T

168520013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551529-T-A

168520145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551663-G-A

168520148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551666-G-A

168520166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551681-A-G

168520351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551864-G-C

http://identifiers.org/hco/6/GRCh38#168520524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14551945-C-A

168520524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551945-C-G

168520524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14551945-C-T

168520834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14552490-G-A

168520838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14552494-T-C

http://identifiers.org/hco/6/GRCh38#168520846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14552502-C-A

168520917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14552548-A-G

168521007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14552631-T-C

168523722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14554096-A-G

168523752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14554125-C-T

168523808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14554178-T-C

168523854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14554222-A-G

168523881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14554247-C-T

168524051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14554385-A-G

168524062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14554396-G-A

168524104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14554438-T-G

168524134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14554449-C-T

168524175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14554475-T-A

168524672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14554943-G-A

168525823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14556439-T-C

168526029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14556565-G-A

168526050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14556585-T-C

http://identifiers.org/hco/6/GRCh38#168526229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14556708-C-A

168526229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14556708-C-T

http://identifiers.org/hco/6/GRCh38#168526238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14556717-C-A

http://identifiers.org/hco/6/GRCh38#168526283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14556756-C-A

168526283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14556756-C-T

168526434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: synonymous variant
orthologous variants: 14556897-C-T

http://identifiers.org/hco/6/GRCh38#168526437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14556900-C-A

168526437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: synonymous variant
orthologous variants: 14556900-C-T

168526473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14556935-G-A

168526473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14556935-G-T

http://identifiers.org/hco/6/GRCh38#168526501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14556960-A-C

168526501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14556960-A-G

168526521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14556980-G-A

168526521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14556980-G-T

168526526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14556985-G-A

168526526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14556985-G-T

168526531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14556990-G-A

168526531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14556990-G-T

168526532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14556991-T-A

168526777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14557202-A-G

168526796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14557221-G-C

168526848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14557266-G-C

168526980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14557368-T-C

168527048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14557420-G-A

http://identifiers.org/hco/6/GRCh38#168527488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14557829-C-A

168527488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14557829-C-G

168527488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14557829-C-T

http://identifiers.org/hco/6/GRCh38#168527535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14557864-A-C

168527535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14557864-A-G

168527535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14557864-A-T

168527714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: synonymous variant
orthologous variants: 14558010-G-A

168527714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: synonymous variant
orthologous variants: 14558010-G-T

http://identifiers.org/hco/6/GRCh38#168527795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14558079-C-A

168527843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14558125-A-T

168527848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14558130-G-A

168527848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14558130-G-C

168527848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14558130-G-T

http://identifiers.org/hco/6/GRCh38#168527879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14558159-C-A

168527879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14558159-C-T

168528109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14558340-T-G

168528290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14558516-T-G

168528391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14558614-A-G

168528393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14558616-G-A

168528555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14558756-A-T

168528599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14558793-T-G

http://identifiers.org/hco/6/GRCh38#168542090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14563203-C-A

168543199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14564178-A-G

168543272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14564258-G-A

168543313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14564280-G-A

168543350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14564301-A-G

168543387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14564339-A-G

http://identifiers.org/hco/6/GRCh38#168543479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14564417-C-A

http://identifiers.org/hco/6/GRCh38#168543638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14564602-A-C

168543642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: synonymous variant
orthologous variants: 14564606-T-C

168543656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: synonymous variant
orthologous variants: 14564620-A-G

168547312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14567640-G-A

168547312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14567640-G-T

168547407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14567697-G-A

168547407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14567697-G-C

168547676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14567852-G-A

168547786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14567924-T-C

168547867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14567999-C-T

168548216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14568324-T-C

168548838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14568697-A-G

http://identifiers.org/hco/6/GRCh38#168549004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14568845-A-C

168549017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14568858-G-A

168549017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14568858-G-T

168549020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14568861-T-C

168549040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14568883-T-A

168549040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14568883-T-C

168549121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 14568959-G-A

168549208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14569045-G-A

168549228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14569065-T-C

168551924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14571131-A-G

168551962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14571168-A-T

168551980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14571186-G-C

168552023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14571222-C-T

168552071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14571270-C-T

168552073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14571272-G-C

168553017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14572001-T-G

168553424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14572298-G-A

168553491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14572362-T-C

http://identifiers.org/hco/6/GRCh38#168553567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14572435-A-C

168553567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14572435-A-G

168553739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14572982-C-G

168553795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14573035-G-A

168556865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14574195-C-G

168556938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14574266-G-A

168565006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14576679-G-A

168565036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14576709-T-C

168565063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14576732-C-T

168565446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577106-G-T

168565451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577111-T-A

168565498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577147-G-A

168565676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577275-C-T

http://identifiers.org/hco/6/GRCh38#168565696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14577295-C-A

168565727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577326-C-T

http://identifiers.org/hco/6/GRCh38#168565809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14577369-C-A

168565809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577369-C-T

168565838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577378-C-G

168565847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577387-A-G

168565869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577409-G-A

168566106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577619-C-T

168566158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577674-T-G

168566177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577693-C-T

168566179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577695-A-G

168566301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577765-C-G

168566310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577775-T-C

http://identifiers.org/hco/6/GRCh38#168566350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14577815-A-C

168566350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577815-A-T

168566378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14577842-G-A

168567099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14578156-T-C

168567197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14578265-A-T

168567359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14578400-C-T

168567374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14578415-A-G

168567374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14578415-A-T

168567378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14578416-G-A

168567449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14578486-T-A

168567470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14578506-T-C

168595519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14587071-G-C

168595716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14587255-A-G

168595828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14587364-G-C

168595878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14587414-G-A

168595878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14587414-G-C

168595878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14587414-G-T

168595900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14587436-G-A

168595914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14587451-A-G

168595982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14587518-A-T

168598840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: missense variant
orthologous variants: 14589192-C-G

168598843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: missense variant
orthologous variants: 14589195-G-C

168598945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: synonymous variant
orthologous variants: 14589297-G-A

168598945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: synonymous variant
orthologous variants: 14589297-G-T

http://identifiers.org/hco/6/GRCh38#168598990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14589342-C-A

168598990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: synonymous variant
orthologous variants: 14589342-C-T

168601041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14590272-C-G

168601143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14590368-C-G

168601170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14590400-G-A

168601241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14590492-C-T

168601242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14590493-G-A

168601274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14590541-G-A

168601274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14590541-G-C

168601274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14590541-G-T

168601362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14590610-C-T

168601686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14590916-A-G

http://identifiers.org/hco/6/GRCh38#168601780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14591010-A-C

168604953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14592573-C-T

168605028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14592645-C-G

168605028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14592645-C-T

168605328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14592911-A-G

168605402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14592987-C-T

168605534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14593107-C-G

168605585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14593159-T-C

168605717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14593242-G-A

168605720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14593245-T-C

168605720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14593245-T-G

168605731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14593253-A-G

http://identifiers.org/hco/6/GRCh38#168605897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14593343-A-C

168605897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14593343-A-G

http://identifiers.org/hco/6/GRCh38#168605931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14593377-C-A

168605931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14593377-C-T

168605935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14593381-T-C

168606021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14593448-A-T

168606368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14593788-A-G

168608292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14595830-T-G

http://identifiers.org/hco/6/GRCh38#168608310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14595849-A-C

168608310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14595849-A-G

168608338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14595854-A-G

168608365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14595885-C-T

http://identifiers.org/hco/6/GRCh38#168608369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14595889-C-A

168608369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14595889-C-G

168608369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14595889-C-T

168608496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14596037-C-T

168608689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14596201-T-A

168608852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14596442-A-G

168608877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14596467-A-G

168608886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14596476-G-A

168608955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14596545-T-C

168609804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14597233-A-G

http://identifiers.org/hco/6/GRCh38#168609998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14597450-C-A

168610524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14597922-C-T

168616147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14599668-G-T

168616197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14599716-C-G

168616197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14599716-C-T

168616198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14599717-G-A

168619045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14600937-C-T

168619065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14600956-G-A

168619154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14601035-T-C

168619859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14601702-G-A

168619860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14601703-G-T

168619943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14601854-C-T

168619997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14601896-T-C

168620082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14601973-G-A

168620521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14602342-G-A

168620689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14602502-C-T

168620839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14602618-G-A

168621078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14602832-C-T

168621080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14602834-C-T

168621165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14602916-G-A

168621194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14602945-G-A

168621275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14603001-G-A

168621275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14603001-G-C

168642679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14613501-G-C

168642861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14613662-C-T

168646375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14614865-T-C

168646392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14614880-C-T

168647151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14615197-G-T

168647289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14615333-G-A

168648738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14616763-G-A

168650453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14617504-T-C

http://identifiers.org/hco/6/GRCh38#168650550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14617644-A-C

168650572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14617665-T-C

168650663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14617754-C-T

http://identifiers.org/hco/6/GRCh38#168650693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14617795-C-A

168650733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: synonymous variant
orthologous variants: 14617835-G-A

168650733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: synonymous variant
orthologous variants: 14617835-G-C

168650754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: synonymous variant
orthologous variants: 14617856-C-T

168652884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron variant
orthologous variants: 14619556-G-A

168653152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 14619831-C-T

http://identifiers.org/hco/6/GRCh38#168653335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14620011-C-A

168653335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14620011-C-T

168653468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14620137-A-G

168663161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14621370-A-G

168663358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14621494-G-A

http://identifiers.org/hco/6/GRCh38#168663472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14621570-C-A

168663472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14621570-C-T

http://identifiers.org/hco/6/GRCh38#168664036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14621770-C-A

168664036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14621770-C-T

168664037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14621771-T-C

http://identifiers.org/hco/6/GRCh38#168664055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14621789-C-A

168664055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14621789-C-T

168664097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 14621827-A-G

168664160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14621896-A-G

168664253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14621965-T-A

168664253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14621965-T-C

http://identifiers.org/hco/6/GRCh38#168664263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14621969-C-A

168664263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14621969-C-G

168664263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14621969-C-T

168664298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14622008-C-T

168664341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14622031-T-C

168664347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14622037-A-T

168664390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14622070-T-A

168664402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14622082-T-A

168664402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14622082-T-C

168664538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14622188-G-T

168664549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14622199-T-C

168664899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14622495-G-C

168665138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14622724-A-T

168665371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14622936-C-T

168665372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14622937-G-A

168665372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14622937-G-C

168665384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14622949-T-A

http://identifiers.org/hco/6/GRCh38#168665676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14623076-A-C

168665762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14623148-A-G

168665811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14623188-A-G

168665917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14623287-T-C

168666291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14623596-A-G

168666306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14623611-G-A

168666306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14623611-G-T

http://identifiers.org/hco/6/GRCh38#168666339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14623659-C-A

168666371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14623690-C-T

168666393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14623711-T-C

168666393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14623711-T-G

168666730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624054-G-A

168666730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624054-G-C

168666730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624054-G-T

168666789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624092-A-G

http://identifiers.org/hco/6/GRCh38#168666815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14624117-A-C

http://identifiers.org/hco/6/GRCh38#168666829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14624131-A-C

168666829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624131-A-G

168667084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624290-C-T

168667095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624301-T-C

http://identifiers.org/hco/6/GRCh38#168667221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14624381-A-C

168667241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624401-G-A

168667241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624401-G-C

168667241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624401-G-T

168667262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624434-T-C

http://identifiers.org/hco/6/GRCh38#168667310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14624455-C-A

168667310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624455-C-G

168667310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624455-C-T

168667540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624653-G-A

168667540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624653-G-T

168667542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624655-A-T

168667611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624724-G-T

http://identifiers.org/hco/6/GRCh38#168667742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14624832-C-A

168667742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624832-C-T

168667784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14624864-G-T

168669673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14626028-T-G

168669753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14626109-T-A

168669783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14626134-C-T

168669784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14626135-C-T

168669939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14626262-T-G

http://identifiers.org/hco/6/GRCh38#168669971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14626291-A-C

168669997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14626317-T-C

http://identifiers.org/hco/6/GRCh38#168670568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14627277-A-C

168670569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14627278-G-A

168670721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14627409-A-G

168670825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14627495-G-A

168670887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14627551-C-T

168670924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14627590-A-T

168671350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14627942-G-A

168671430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14627982-C-G

168671430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14627982-C-T

168671436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14627988-G-A

http://identifiers.org/hco/6/GRCh38#168671765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14628049-A-C

168671866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14628123-C-T

168671923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14628169-C-T

168671952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14628195-A-G

168672209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14628441-T-G

168672210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14628442-G-A

http://identifiers.org/hco/6/GRCh38#168672291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#14628522-C-A

168672314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14628565-C-T

168672412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: non coding transcript exon variant
orthologous variants: 14628667-T-C

168672412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: non coding transcript exon variant
orthologous variants: 14628667-T-G

168672516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20323
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14628771-G-A