186286135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696700-A-G

186286200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696638-C-T

186286241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696591-G-A

186286241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696591-G-C

186286241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696591-G-T

http://identifiers.org/hco/4/GRCh38#186286243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45696589-C-A

186286243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696589-C-T

http://identifiers.org/hco/4/GRCh38#186286244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45696588-A-C

186286244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696588-A-G

186286244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696588-A-T

186286248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696584-G-A

186286248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45696584-G-T

186286301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696536-A-T

186286324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696513-A-G

186286342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696495-G-A

186286342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696495-G-T

186286461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45695950-A-G

186286500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45695911-A-G

http://identifiers.org/hco/4/GRCh38#186286597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45695802-A-C

186286779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45695658-T-G

186286902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45695538-C-T

186286917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45695522-G-T

186287617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45695440-T-C

186287625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45695432-T-C

186287725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45695350-G-A

http://identifiers.org/hco/4/GRCh38#186287773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#45695302-C-A

186287821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 45695254-A-G

186288197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45694855-C-G

186288251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45694844-A-G

186288299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45694796-A-G

186288304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45694791-G-A

186288304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45694791-G-T

186288340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45694755-A-G

186288348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45694747-G-A

186288576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 45694521-T-G

186288622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 45694473-C-T

http://identifiers.org/hco/4/GRCh38#186288623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#45694472-C-A

186288623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 45694472-C-T

186288629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 45694466-G-A

http://identifiers.org/hco/4/GRCh38#186288688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#45694400-C-A

186288695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 45694395-G-A

186288695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 45694395-G-C

http://identifiers.org/hco/4/GRCh38#186288696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#45694394-C-A

http://identifiers.org/hco/4/GRCh38#186288702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#45694388-C-A

186288702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 45694388-C-T

http://identifiers.org/hco/4/GRCh38#186288713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#45694377-C-A

186288713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 45694377-C-T

186288719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 45694371-A-T

186288771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 45694333-T-A

186288771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 45694333-T-C

186288908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 45694219-T-C

186288908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 45694219-T-G

186289232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45692959-A-G

186289233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45692958-G-A

186289502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45692681-A-T

186289584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45692625-T-C

186290092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45692419-A-G

186290261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45692257-A-G

186290357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45692222-T-C

186290417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45692170-T-C

186290726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691878-T-C

http://identifiers.org/hco/4/GRCh38#186290751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45691853-C-A

186290751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691853-C-G

186290751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691853-C-T

186297264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691411-C-T

186297825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690527-T-A

186297825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690527-T-C

186297836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690516-C-G

186297873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690469-T-A

186297873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690469-T-G

186297941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690423-T-A

186297941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690423-T-G

http://identifiers.org/hco/4/GRCh38#186297948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45690416-C-A

186297956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690408-T-A

186297979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690396-T-A

186297979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690396-T-G

186298003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690382-G-A

186298003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690382-G-C

186298003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690382-G-T

186298358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690026-G-C

186298375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689966-G-A

186298416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689926-T-C

186298434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689907-A-T

186298496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689840-G-A

http://identifiers.org/hco/4/GRCh38#186298534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45689801-C-A

186298534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689801-C-G

186339456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45664067-T-C

186339583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45663961-G-T

186340452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45661842-G-A

186340469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45661827-T-C

http://identifiers.org/hco/4/GRCh38#186340481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45661815-C-A

186340481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45661815-C-T

186340482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45661814-C-T

186340741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45661587-A-T

186340945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45661296-T-C

186340976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45661265-T-C

186341240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45661013-T-G

http://identifiers.org/hco/4/GRCh38#186341488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45657520-C-A

186341488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45657520-C-T

186341572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45657457-G-A

186341572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45657457-G-C

186347417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45655474-A-G

186347492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45655408-C-T

186347522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45655378-G-T

186347549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45655351-A-G

186347569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45655331-G-A

186347569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45655331-G-T

186347607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45655284-C-T

186347627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45655264-T-C

186347658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45655233-G-A

186347886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45654876-T-C

186348136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45654641-C-T

186348395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45654409-C-T

http://identifiers.org/hco/4/GRCh38#186348396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45654408-A-C

186348399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45654405-A-T

186348537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45654280-G-A

http://identifiers.org/hco/4/GRCh38#186348565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45654252-A-C

186348694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45654122-T-C

186348744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45654073-T-A

186348911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45653907-G-A

186349245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45650858-A-G

186349300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45650788-C-T

186349392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45650733-T-G

186349470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45650617-T-C

186349520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45650579-G-C

186349697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45650432-C-T

186349721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45650408-C-T

186349817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45650302-C-T

http://identifiers.org/hco/4/GRCh38#186349848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45650267-C-A

186349848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45650267-C-G

http://identifiers.org/hco/4/GRCh38#186351740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45649298-C-A

186352004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45649045-T-A

186352168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45648877-A-G

http://identifiers.org/hco/4/GRCh38#186352170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45648875-C-A

186352889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45648223-A-T

186352893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45648219-G-T

186352991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45648146-T-A

186353212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45647905-C-T

186353396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45647731-C-T

http://identifiers.org/hco/4/GRCh38#186353491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45647638-C-A

186353491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45647638-C-T

186353657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45647582-G-A

186354170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45647294-T-C

186354323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45647150-G-T

186354602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45646899-T-A

186354603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45646898-C-G

186354603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45646898-C-T

186354605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45646896-T-C

186354693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45646807-T-C

186354877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45646499-A-G

186355121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45646266-T-C

186355121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45646266-T-G

http://identifiers.org/hco/4/GRCh38#186362003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45644725-C-A

186362233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45644523-T-C

186362279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45644478-C-T

186362333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45644426-A-G

186362502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45644289-C-G

186362526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45644277-G-A

186362526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45644277-G-T

186362662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45644141-T-A

186362662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45644141-T-C

186362761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45644044-C-T

186364637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45643221-C-T

186364695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45643153-G-A

http://identifiers.org/hco/4/GRCh38#186365298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45641910-C-A

186365298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45641910-C-G

186365361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45641856-A-G

186365399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45641818-T-C

186365423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45641795-A-G

186365449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45641774-A-T

186365633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45641586-A-G

186367050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45638842-C-T

186367084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45638820-T-A

186367236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45638667-T-C

186367271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45638639-C-T

186367691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45631782-A-G

186367763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45631725-A-G

186367805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45631694-C-G

186368045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45631551-T-G

186372905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45631340-A-G

186372948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45631299-C-T

186372974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45631264-A-G

186373140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45630769-C-T

http://identifiers.org/hco/4/GRCh38#186401471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45620576-A-C

186405176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45619412-T-G

186407203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45614488-G-A

186407277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45614408-C-T

186407290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45614395-T-C

186407368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45614332-C-G

186407417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45614282-A-G

186407489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45614208-G-A

186407534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45614173-G-A

186407577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45614130-A-G

http://identifiers.org/hco/4/GRCh38#186407738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45613963-C-A

186407889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45613810-G-A

186407980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45613720-T-C

186408044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45613654-C-G

186409651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45612426-G-A

186409665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45612407-C-G

186409934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45612208-A-G

186410368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45610233-C-T

186410512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45610107-C-G

186410512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45610107-C-T

186410530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45610092-T-C

186410705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45609867-A-T

186410717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45609855-G-A

186416606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45603704-G-C

186417237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45603198-T-G

186417291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45603142-G-A

186417291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45603142-G-C

186417300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45603133-A-G

186422229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45593093-G-T

186423453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45592517-A-G

186423501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45592470-T-C

186423608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45592363-T-C

186423754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45592239-G-A

186423754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45592239-G-T

http://identifiers.org/hco/4/GRCh38#186423966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45592047-C-A

186424000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45592011-T-C

186424000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45592011-T-G

186424068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45591943-G-T

186424071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45591940-T-C

186424746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45590732-T-A

186424748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45590730-G-A

186424752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45590541-G-C

186424943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45590286-G-A

186424982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45590240-T-A

186425124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45590099-G-A

http://identifiers.org/hco/4/GRCh38#186425207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45590007-A-C

186425252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45589964-A-G

186425253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45589963-T-C

186425301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45589930-T-A

186425325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45589906-G-A

186426176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45589730-T-C

186426180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45589726-T-C

186426180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45589726-T-G

186426181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45589725-G-A

186426181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45589725-G-C

186426181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45589725-G-T

186426230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45589679-G-T

186426283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45589643-A-G

http://identifiers.org/hco/4/GRCh38#186426383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45589536-C-A

186426391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45589528-T-G

186426432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45589496-G-A

186426432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45589496-G-C

186426635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45589294-G-T

186426637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45589292-T-C

186426698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45589226-T-A

186426762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45589165-C-T

186426804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45589127-G-T

186426871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45589063-T-C

http://identifiers.org/hco/4/GRCh38#186426921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45589016-C-A

186426921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45589016-C-T

186426987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45588953-C-T

186427007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45588933-G-A

186427029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45588911-T-C

186427052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45588888-T-C

186427057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45588883-A-G

186427057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45588883-A-T

http://identifiers.org/hco/4/GRCh38#186427170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45588772-C-A

186427170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45588772-C-G

186427170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45588772-C-T

186427305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45588612-G-A

186427370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45588542-A-G

186427447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45588466-A-T

186427597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45588308-G-A

186443576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

186461586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45579269-A-G

186461604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45579251-C-T

186461790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45579075-C-T

186461936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578922-T-C

186463140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578463-A-G

186463171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578432-G-A

186463188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578415-T-C

186463188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45578415-T-G

186464506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45577636-A-G

186464587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45577533-G-A

186464733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45577356-T-G

186464786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45577328-G-A

186464854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45577267-G-A

http://identifiers.org/hco/4/GRCh38#186464909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45577209-C-A

186464909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45577209-C-T

186464998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45577119-C-T

186465002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45577115-A-G

186465351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574775-A-G

186465355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574771-A-G

186465467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574666-A-G

186465549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574648-T-A

186465549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574648-T-G

http://identifiers.org/hco/4/GRCh38#186465554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45574653-C-A

186465554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574653-C-G

186465554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574653-C-T

186465567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574666-T-A

186465567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574666-T-C

186465567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574666-T-G

186465599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574697-A-T

186465621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574717-T-A

186465658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574750-A-G

186465746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574836-T-C

http://identifiers.org/hco/4/GRCh38#186466103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45574528-C-A

186466103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574528-C-T

186466120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574524-G-A

186466120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574524-G-C

186466219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574455-T-C

186466226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574448-G-A

186466226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574448-G-C

186466423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574224-G-A

186466544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45574109-C-T

186466771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45573964-G-A

186466771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45573964-G-C

186466931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45573943-A-T

186467023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45573843-G-A

186467115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45573736-C-T

186467193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45573675-T-C

http://identifiers.org/hco/4/GRCh38#186467257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45573617-A-C

186469616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45572671-T-C

186473323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45572375-T-C

186473418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45572290-C-G

186473482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45572226-T-C

186480729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45571463-C-G

186480818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45571381-G-C

186480951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45571058-A-G

186480985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45571024-C-T

186481072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570947-A-G

186481173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570834-A-G

186481225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570782-G-A

186481376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570639-A-G

186481418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570599-C-T

186481445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570574-C-G

186481560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570475-G-C

186481654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45570382-C-T

http://identifiers.org/hco/4/GRCh38#186482317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#45569822-C-A

186482344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45569795-T-C

186482344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45569795-T-G

186482499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45569472-G-A

186482499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45569472-G-T

186482575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45569408-T-C

186482741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45568828-A-G

186486179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45563246-T-C

http://identifiers.org/hco/4/GRCh38#186486230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45563200-A-C

186486415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45563017-G-A

186486433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45562998-G-A

186486438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45562993-G-A

186486484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45562954-G-A

186486484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45562954-G-T

186486524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45562914-C-G

186486668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45562750-G-A

186486694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45562721-G-A

186486701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45562714-G-A

186486702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45562713-G-C

186486811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45562623-G-T

186486864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45562577-G-T

186488160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45561781-T-C

186488224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27725
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45561723-A-T