40315989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120325564-C-T

40317225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120325916-C-T

40317275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120325963-G-T

http://identifiers.org/hco/3/GRCh38#40317318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120325996-C-A

40317980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120326426-A-G

40327882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120330524-A-G

40327893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120330539-G-C

40327922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120330568-G-A

40327922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120330568-G-C

40327924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120330570-G-A

40327961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120330608-G-A

40327961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120330608-G-C

40328019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120330658-T-A

40328019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120330658-T-G

40328165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120330821-C-T

40328265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120330907-G-A

http://identifiers.org/hco/3/GRCh38#40332458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#120333426-A-C

40332604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120333568-G-A

40332622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120333585-A-G

40333052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120334971-G-C

http://identifiers.org/hco/3/GRCh38#40333202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#120335087-C-A

40333808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120336675-A-G

40334053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120336930-T-C

40334084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120336969-C-T

40334284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120337168-G-A

40334491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120337372-C-T

40334551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120337460-G-A

40361987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120345516-G-A

40362217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120345671-T-C

40362253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120345710-T-A

http://identifiers.org/hco/3/GRCh38#40362441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#120345878-C-A

40362447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120345884-T-C

40362481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120345913-A-G

40362503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120345935-T-A

40362503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120345935-T-C

40362612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120346034-T-C

40362637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120346062-C-G

40362637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120346062-C-T

40363059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120346615-C-T

40363141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120346688-T-A

40363141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120346688-T-C

40363182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120346728-A-G

40363376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120346937-A-G

40364717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120354585-T-C

40364815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120354683-T-C

40365011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120354889-G-A

http://identifiers.org/hco/3/GRCh38#40366689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#120356201-A-C

40366689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120356201-A-G

40366901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120356390-C-T

40366902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120356391-C-T

40367021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120356509-C-G

40367051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120356539-T-C

40385344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120365724-G-C

40385369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120365753-G-A

40385455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120365837-C-T

40385485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120365857-T-C

40385888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120366201-T-C

40387062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120368786-G-T

40387201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120368898-G-A

40387277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120368962-C-T

http://identifiers.org/hco/3/GRCh38#40387305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120368982-C-A

40387305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120368982-C-G

40387305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120368982-C-T

http://identifiers.org/hco/3/GRCh38#40387313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120368990-C-A

40387313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120368990-C-T

40387332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369009-G-A

40387332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369009-G-T

40387383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369059-T-C

40387430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369082-G-A

40387430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369082-G-C

40387430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369082-G-T

http://identifiers.org/hco/3/GRCh38#40387436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120369090-C-A

40387436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369090-C-T

http://identifiers.org/hco/3/GRCh38#40387451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120369105-C-A

40387451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369105-C-G

40387451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369105-C-T

40387695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369311-A-G

40387872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369577-T-A

40387872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369577-T-C

http://identifiers.org/hco/3/GRCh38#40387890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120369594-C-A

40387890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369594-C-T

http://identifiers.org/hco/3/GRCh38#40387919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120369621-C-A

40387919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369621-C-T

40387952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369653-G-A

40387952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369653-G-T

40387969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369666-T-C

40388137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369804-A-T

http://identifiers.org/hco/3/GRCh38#40388142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120369809-C-A

http://identifiers.org/hco/3/GRCh38#40388151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120369818-C-A

40388151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369818-C-G

http://identifiers.org/hco/3/GRCh38#40388152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120369819-C-A

40388165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369832-A-G

40388178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369845-C-T

40388180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369847-T-C

40388307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120369969-G-A

40388338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120370000-G-C

40388889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120370725-A-G

40389760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120371489-G-T

40389774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120371503-G-C

40389813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120371541-G-A

40390018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120371738-A-G

40390072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120371781-T-G

40390664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120372526-T-G

40390774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120372688-T-A

40390780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120372694-T-C

40392214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120373179-T-C

http://identifiers.org/hco/3/GRCh38#40392258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120373218-C-A

40392292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120373242-G-A

40392988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120373556-G-A

40393306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120373820-C-T

40393470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120373973-T-C

40393503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120374006-A-T

40394434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120374634-A-G

40394440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120374640-T-A

40394480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120374681-T-C

http://identifiers.org/hco/3/GRCh38#40394496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120374717-C-A

40394499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120374720-T-C

40396061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120376031-T-A

40396107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120376076-C-G

40396173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120376127-G-A

40396173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120376127-G-C

40396267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120376216-T-C

40396306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120376251-T-A

40396444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120376403-T-C

40396731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120376671-T-C

40397086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120376985-C-T

40397101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120377000-G-T

40397166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120377050-A-T

40397322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120377144-G-T

40397605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120377335-T-C

40397694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120377426-G-T

40398399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120379916-G-A

40398399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120379916-G-C

40398404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120379921-T-C

40398772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120380226-T-C

40398931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120380361-T-C

40399384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120381473-G-A

40399456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120381543-A-G

40399477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120381560-G-T

40399573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120381631-G-A

40399577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120381634-C-T

http://identifiers.org/hco/3/GRCh38#40399651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120381688-C-A

40399684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120381710-G-T

40399708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120381734-G-T

40399714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120381740-G-A

40399714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120381740-G-T

40399790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120381793-C-T

40400820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120383065-T-C

40400842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120383087-G-A

40400849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120383094-G-A

40400849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120383094-G-C

40401131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120383291-G-A

40401289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120383425-A-G

40401411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120383533-A-T

40401434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120383555-T-C

http://identifiers.org/hco/3/GRCh38#40411800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120384699-C-A

http://identifiers.org/hco/3/GRCh38#40411999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120384897-A-C

http://identifiers.org/hco/3/GRCh38#40412229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120385094-C-A

40412484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120385332-T-C

40414640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120386417-T-G

40414795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120386572-A-G

40414885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120386662-T-C

40414885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120386662-T-G

40414886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120386663-A-G

40414912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120386692-G-A

http://identifiers.org/hco/3/GRCh38#40414918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120386698-C-A

40414918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120386698-C-G

40414918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120386698-C-T

40414987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120386723-A-G

40414987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120386723-A-T

40415574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120387161-T-C

40415692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120387259-A-G

40415717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120387281-G-T

http://identifiers.org/hco/3/GRCh38#40415739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120387302-C-A

http://identifiers.org/hco/3/GRCh38#40415789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120387351-C-A

40415789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120387351-C-G

40415878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120387440-G-A

http://identifiers.org/hco/3/GRCh38#40415929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120387491-C-A

40415929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120387491-C-T

http://identifiers.org/hco/3/GRCh38#40415962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120387524-C-A

40415962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120387524-C-T

40415983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120387545-G-C

40416025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120387587-C-T

40416070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120387632-G-A

40416070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120387632-G-T

40416116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120387651-G-C

http://identifiers.org/hco/3/GRCh38#40416127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120387664-A-C

40416182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120387711-G-A

40422829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120389526-A-G

http://identifiers.org/hco/3/GRCh38#40422861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120389558-C-A

40422861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120389558-C-T

40422994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120389691-G-T

40423195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120389915-G-A

40423198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120389918-G-A

40423198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120389918-G-T

http://identifiers.org/hco/3/GRCh38#40423206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120389926-A-C

40423206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120389926-A-G

40423255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120389959-T-G

40423268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120389969-T-G

40423335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120390031-A-G

40423388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120390084-A-G

40423388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120390084-A-T

40423449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120390144-T-C

40423716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120390876-A-G

40423716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120390876-A-T

40423752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120390909-T-C

http://identifiers.org/hco/3/GRCh38#40423800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120390936-C-A

40424026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120391151-G-C

40424169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120391264-G-A

40424310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120391393-T-C

40424440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120391818-G-A

40424776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120392580-A-T

40424999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120392788-A-G

40425012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120392801-G-A

40425012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120392801-G-T

40426854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120395036-A-T

40426942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120395122-T-G

http://identifiers.org/hco/3/GRCh38#40426990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120395168-C-A

40427120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120395250-A-G

http://identifiers.org/hco/3/GRCh38#40427147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120395272-C-A

40427147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120395272-C-T

40427158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120395283-T-C

40427158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120395283-T-G

http://identifiers.org/hco/3/GRCh38#40427367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120395467-A-C

40427370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120395470-A-G

40427493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120395593-A-T

40427568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120395666-G-A

40427568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120395666-G-T

40427716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120395807-A-G

40427783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120395873-T-A

40427783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120395873-T-G

40427851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120395931-C-T

http://identifiers.org/hco/3/GRCh38#40427857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#120395937-C-A

40427948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120396054-T-C

40428044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120396253-C-T

40428045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120396254-A-G

40428251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120396551-A-G

40428305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120396614-G-A

40428305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120396614-G-T

40428569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26710
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120396837-A-G