43909304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117530614-A-G

43909378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117530556-T-G

43909502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117530447-G-T

43909566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117530334-G-A

43909591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117530309-A-G

43909670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117530235-T-G

43909810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117530106-T-C

43909868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117530043-G-A

43909868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117530043-G-T

43910233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117529733-T-C

43910581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117529393-T-C

43910693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117529099-A-G

43910727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117528970-G-A

http://identifiers.org/hco/10/GRCh38#43911167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117528502-C-A

http://identifiers.org/hco/10/GRCh38#43911404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117528207-C-A

43911412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117528199-G-A

43925179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117524811-C-T

43925469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117524551-T-G

43925477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117524543-G-A

43925477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117524543-G-C

43925635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117524312-A-G

43925667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117524289-C-G

43925667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117524289-C-T

43931303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117522024-T-C

43931408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117521904-T-G

43931469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117521843-G-T

43931504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117521808-A-T

43931769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117521564-G-C

43938955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117512274-C-T

43939006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117512211-A-G

43939007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117512210-T-C

http://identifiers.org/hco/10/GRCh38#43939029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117512189-C-A

43939029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117512189-C-G

43939048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117512170-C-T

43939086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117512125-G-A

43939086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117512125-G-T

43939144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117512063-A-G

43939737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511632-G-A

43939766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511603-G-T

43939793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511577-G-T

43939796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511574-T-A

43939805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511565-T-A

43939805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511565-T-G

43939807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511563-T-C

43939807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511563-T-G

43939818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511550-G-T

43939839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511530-G-A

43939839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511530-G-T

43939849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511520-G-A

43939849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511520-G-T

43939917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511453-A-G

43940014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511370-A-G

43940030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511357-G-A

43940036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511351-A-G

43940041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511346-G-A

43940041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511346-G-C

43940041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511346-G-T

43940097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511292-T-C

43940223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511178-A-G

43940225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511176-G-T

43940354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511044-T-C

43940391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511010-A-G

43940391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117511010-A-T

http://identifiers.org/hco/10/GRCh38#43940439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117510994-C-A

43940439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117510994-C-G

43940468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117510958-G-A

43940540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 117510898-A-G

43940550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 117510889-T-C

43940575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117510867-A-G

http://identifiers.org/hco/10/GRCh38#43940604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117510839-C-A

43940604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117510839-C-T

43940618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117510825-G-A

http://identifiers.org/hco/10/GRCh38#43940673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117510771-C-A

43940683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117510761-T-C

43940743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117510718-T-C

43940743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117510718-T-G

43940767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117510668-C-T

43940780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117510655-A-G

43940835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117510612-T-C

43941270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117510417-T-C

43941330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117510355-C-T

43941439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117510240-C-T

43941599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117510010-G-A

43941639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117509971-C-T

43941687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117509922-T-G

43941758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117509856-A-G

43941811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117509806-A-G

43941904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117509714-T-A

43941904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117509714-T-C

43943663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117509270-A-G

43943686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117509247-T-A

43943686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117509247-T-C

http://identifiers.org/hco/10/GRCh38#43944042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117504932-C-A

43944042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117504932-C-G

43944058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117504916-G-A

43944058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117504916-G-T

43944071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117504903-C-T

43944147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117504820-G-T

http://identifiers.org/hco/10/GRCh38#43944227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117504721-C-A

43944237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117504711-G-T

43944253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117504693-T-C

43944254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117504692-C-T

43944258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117504688-A-T

43944266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117504680-G-T

http://identifiers.org/hco/10/GRCh38#43944278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117504668-C-A

43944288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117504657-C-T

http://identifiers.org/hco/10/GRCh38#43944305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117504641-C-A

43944305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117504641-C-G

43944305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117504641-C-T

http://identifiers.org/hco/10/GRCh38#43944329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117504617-C-A

43944329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117504617-C-G

43944374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117504571-A-G

43944627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117504318-A-G

43944785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117504145-C-T

43944925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117503995-C-T

43944981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117503941-T-C

43945142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117503789-T-G

43945236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117503707-G-A

43945288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117503657-C-T

43945365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117503582-G-A

43945434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117503503-G-T

43945505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117503438-C-T

43945568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117503385-A-G

43945743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117503239-C-T

43945783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117503193-A-G

43945840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117503103-T-C

43945941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117503012-G-A

43946105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117502858-A-G

43946117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117502847-G-T

43946213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117502753-G-C

43953513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117494437-G-A

43953638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117494318-C-G

43953676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117494284-G-T

43953717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117494243-G-A

43954251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117493789-C-T

http://identifiers.org/hco/10/GRCh38#43954493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117493541-C-A

43954507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117493524-G-T

43955172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117493085-C-G

43955355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117492926-A-G

43955414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117492877-C-T

43955529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117492779-C-T

43955640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117492665-T-A

43955803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117492503-G-T

43957551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117492164-G-A

43957651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117492064-G-A

43957670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117492045-C-T

43958011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117491760-G-A

43958133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117491677-G-A

43958293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117491522-G-T

43958330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117491485-C-G

43958330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117491485-C-T

43958331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117491484-G-A

43958351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117491445-C-G

43958357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117491439-A-G

43958752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117491015-C-T

43958871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117490889-C-T

43958993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117490765-C-G

http://identifiers.org/hco/10/GRCh38#43959060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117490685-A-C

43959060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117490685-A-G

43959061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117490684-C-G

43959061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117490684-C-T

43959286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117490470-A-G

http://identifiers.org/hco/10/GRCh38#43959294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117490462-C-A

43959401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117490375-C-T

43959420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117490361-G-A

43959420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117490361-G-T

43959422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117490359-G-T

43959484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117490293-G-A

43959492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117490288-A-T

43959503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117490277-C-G

43959508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117490272-C-T

http://identifiers.org/hco/10/GRCh38#43959570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117490220-A-C

43959611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117490167-C-T

43959822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117489588-A-G

43959966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117489464-C-G

http://identifiers.org/hco/10/GRCh38#43959980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117489450-C-A

43960006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117489425-C-T

43960154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117489276-G-C

43960392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117489000-T-C

43960564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117488855-G-A

43960581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117488838-G-T

http://identifiers.org/hco/10/GRCh38#43960745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117488665-A-C

43960941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117488491-C-G

43961476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117487751-A-G

43961545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117487683-A-G

43961712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117487522-G-A

43961727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117487486-C-T

43961751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117487462-G-C

http://identifiers.org/hco/10/GRCh38#43961976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117487258-C-A

43961993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117487241-T-C

43962003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117487231-C-T

http://identifiers.org/hco/10/GRCh38#43962206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117486764-C-A

43962206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117486764-C-T

43962421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117486572-C-G

43962421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117486572-C-T

43962433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117486557-C-G

43962433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117486557-C-T

43962655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117486351-G-A

43962718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117486305-T-C

43962773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117486241-G-A

43962928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117486075-C-T

43963145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117485856-C-T

43963426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117485566-T-G

43963574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117485439-T-A

http://identifiers.org/hco/10/GRCh38#43963643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117485379-C-A

43963698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117485340-G-A

http://identifiers.org/hco/10/GRCh38#43963875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117485188-C-A

43963954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117485117-T-A

43964006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117485063-G-A

43964035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117485039-T-A

43964150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117484931-G-A

43964257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117484290-C-T

43964288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117484259-G-A

43964288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117484259-G-T

43964325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117484236-C-T

43964326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117484235-T-C

43964441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117484135-G-A

http://identifiers.org/hco/10/GRCh38#43964540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117484046-A-C

http://identifiers.org/hco/10/GRCh38#43964620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117483972-C-A

43964620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117483972-C-T

43964633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117483959-G-A

http://identifiers.org/hco/10/GRCh38#43964657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117483935-A-C

43964696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117483896-T-G

43964717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117483875-A-G

43964766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117483827-C-T

43964784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117483808-C-T

http://identifiers.org/hco/10/GRCh38#43964796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117483796-C-A

43964822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117483770-G-A

43964822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117483770-G-T

43964913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117483691-T-C

43964964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117483641-G-A

43965256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117482989-G-A

43965392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117482871-G-A

43965432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117482832-A-G

43965562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117482709-G-C

43965612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117482671-A-G

http://identifiers.org/hco/10/GRCh38#43965778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117482534-A-C

43965830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117482482-G-A

43965830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117482482-G-C

43965971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117482321-T-C

http://identifiers.org/hco/10/GRCh38#43966010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117482282-C-A

http://identifiers.org/hco/10/GRCh38#43966161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117482124-C-A

43966251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117482020-C-T

43966486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117481822-A-T

43967734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117478013-G-A

43967942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117477699-G-T

43967956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117477685-A-G

43968027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117477640-C-G

43968217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117477444-T-C

43968335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117477316-C-G

43968361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117477292-G-C

43968423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117477231-G-T

43968447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117477207-A-G

43968488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117477161-C-T

43968787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117476864-T-C

43968906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117476742-A-G

43974657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117472522-G-A

43974762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117472423-C-T

43974875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117472309-C-G

43974914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117472271-T-A

43974983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117472189-T-C

43975084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117472116-T-A

43975428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117471821-G-A

43975455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117471794-C-T

43975509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117471738-C-G

43975509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117471738-C-T

http://identifiers.org/hco/10/GRCh38#43975520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117471727-C-A

43975676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117471573-T-G

43975989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117471281-A-G

43976333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117470998-T-A

43976490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117470881-G-A

43976490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117470881-G-C

43977072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117470247-A-G

43977163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117470154-G-A

43977177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117470140-T-C

43977193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117470124-A-G

43977193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117470124-A-T

43977209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117470109-G-A

43977226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117470092-G-C

43977231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117470087-T-C

43977455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117469887-G-A

43977647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117469703-T-C

43977682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117469667-G-T

http://identifiers.org/hco/10/GRCh38#43977716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#117469633-A-C

43977751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117469598-A-G

43977832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117469518-A-G

43978063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117469300-T-C

43980467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: non coding transcript exon variant
orthologous variants: 117468469-T-C

43980484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: non coding transcript exon variant
orthologous variants: 117468452-G-T

43980658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: non coding transcript exon variant
orthologous variants: 117468291-G-A

43980708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27430
most severe consequence: non coding transcript exon variant
orthologous variants: 117468241-G-C