18805165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117730836-G-A

18805278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117730950-A-G

18805903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117731538-A-G

http://identifiers.org/hco/16/GRCh38#18805932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117731567-C-A

18806037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117731669-G-T

http://identifiers.org/hco/16/GRCh38#18806076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117731706-C-A

http://identifiers.org/hco/16/GRCh38#18806108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117731738-C-A

18806108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117731738-C-G

http://identifiers.org/hco/16/GRCh38#18806222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117731842-C-A

18806222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117731842-C-T

http://identifiers.org/hco/16/GRCh38#18806245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117731865-A-C

http://identifiers.org/hco/16/GRCh38#18806260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117731880-C-A

18806260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117731880-C-T

18806308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117731927-G-A

18806308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117731927-G-C

18806308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117731927-G-T

18806408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117732025-C-T

18806491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117732085-A-G

18806883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117732499-C-T

18807067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117732640-G-C

18807067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117732640-G-T

18807173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117732752-A-G

18807180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117732759-C-T

18807285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117732853-G-T

18807464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117733017-T-C

18807608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117733140-C-T

18807609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117733141-G-A

18807609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117733141-G-C

18807686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117733193-A-G

18807686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117733193-A-T

18808080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117733269-G-T

18808360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117733513-T-C

18808907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117734122-G-T

18809318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117734523-G-A

18809318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117734523-G-T

18811733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117735881-G-A

18811997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117736146-A-G

18812200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117736342-G-A

18812200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117736342-G-T

18812202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117736344-A-G

18815318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117738782-T-G

18815325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117738790-T-C

18815686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117739148-T-C

18815722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117739183-A-G

18816013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117739418-G-T

http://identifiers.org/hco/16/GRCh38#18816080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117739454-C-A

18816122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117739490-T-C

http://identifiers.org/hco/16/GRCh38#18816127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117739495-C-A

18816127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117739495-C-T

18816296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117739647-T-C

18816443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: synonymous variant
orthologous variants: 117739794-C-T

18816787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117740092-G-A

18816839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117740144-G-A

18816917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117740225-T-C

18816939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117740249-C-G

18816959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117740269-G-A

18817011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117740310-C-T

http://identifiers.org/hco/16/GRCh38#18817555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117740773-A-C

18817555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117740773-A-G

18817583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117740800-G-C

18817583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117740800-G-T

18819577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: synonymous variant
orthologous variants: 117741018-A-G

18819706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117741145-T-C

18819714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117741153-G-A

18819714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117741153-G-C

18819714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117741153-G-T

http://identifiers.org/hco/16/GRCh38#18819791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117741220-A-C

18819791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117741220-A-T

18819846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117741271-T-A

18819846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117741271-T-C

18828006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117742458-G-A

18828006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117742458-G-T

18828184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117742631-G-A

18828184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117742631-G-C

18828184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117742631-G-T

18828201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117742647-G-A

18828201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117742647-G-T

18828240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117742684-G-A

18828240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117742684-G-T

18828354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117742774-C-G

18828380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117742800-T-A

18828380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117742800-T-C

18828380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117742800-T-G

18828486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117744041-G-A

18828524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117744079-G-T

18829116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117744420-A-G

18829153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117744453-G-A

18829153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117744453-G-C

18829153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117744453-G-T

18829179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117744479-G-A

18829179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117744479-G-C

18829179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117744479-G-T

18829188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117744488-G-C

18829188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117744488-G-T

18829212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117744510-G-A

18829212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117744510-G-T

http://identifiers.org/hco/16/GRCh38#18829304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117744572-C-A

18829448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: missense variant
orthologous variants: 117744716-C-G

18829451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: missense variant
orthologous variants: 117744719-G-C

18829451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: synonymous variant
orthologous variants: 117744719-G-T

18829476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: missense variant
orthologous variants: 117744744-C-G

18829610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: synonymous variant
orthologous variants: 117744878-G-C

18829901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117745175-A-G

18830115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 117745380-A-G

18830115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 117745380-A-T

http://identifiers.org/hco/16/GRCh38#18830175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117745435-C-A

18830175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117745435-C-G

18830333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: synonymous variant
orthologous variants: 117745588-C-T

http://identifiers.org/hco/16/GRCh38#18830381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117745636-C-A

18832089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117746872-G-A

18832116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117746889-C-G

18832685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117747594-T-C

18832797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117747694-A-T

18832884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117747786-T-G

18833047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: synonymous variant
orthologous variants: 117748064-G-A

18833068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: synonymous variant
orthologous variants: 117748085-G-A

http://identifiers.org/hco/16/GRCh38#18834233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117751530-A-C

18834233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: synonymous variant
orthologous variants: 117751530-A-G

18835152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: missense variant
orthologous variants: 117752160-T-A

18835152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: synonymous variant
orthologous variants: 117752160-T-C

http://identifiers.org/hco/16/GRCh38#18835213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117752217-C-A

18835213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117752217-C-T

18835255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117752279-A-G

18835255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117752279-A-T

18835256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117752280-G-A

18835256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117752280-G-C

18835256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117752280-G-T

18836242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117753691-T-C

18836664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117754093-T-C

18836664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117754093-T-G

18836666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117754095-T-A

18836666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117754095-T-G

18836882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117754290-G-A

http://identifiers.org/hco/16/GRCh38#18837172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117755060-C-A

18837172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117755060-C-G

18837172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117755060-C-T

http://identifiers.org/hco/16/GRCh38#18837221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117755113-C-A

18837221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117755113-C-T

18837409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: missense variant
orthologous variants: 117755305-A-G

18837460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117755353-C-T

18837465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117755358-A-G

http://identifiers.org/hco/16/GRCh38#18837529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117755398-A-C

18838281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117756004-C-T

18838750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117756467-G-T

18838755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117756472-T-C

18838791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117756509-T-A

18838791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117756509-T-C

18838798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117756516-T-C

18839430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117756974-G-A

18839547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117757081-A-G

18839547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117757081-A-T

http://identifiers.org/hco/16/GRCh38#18839564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117757098-C-A

18839651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117757166-G-A

18839651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117757166-G-T

18840018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117757638-G-A

18840212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117757883-T-A

18840244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117757905-C-T

18840294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117757949-C-G

18840695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117758311-T-C

18840993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117758494-A-G

http://identifiers.org/hco/16/GRCh38#18841379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117758595-C-A

18841401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117758612-A-G

http://identifiers.org/hco/16/GRCh38#18841478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117758709-A-C

18841478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117758709-A-G

18841478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117758709-A-T

18841488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117758719-A-G

18841552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117758799-T-A

18841688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117758937-T-C

18841901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117759115-G-A

18841901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117759115-G-T

18841948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117759158-G-A

18842098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117759257-A-G

18842144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117759317-A-G

18842144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117759317-A-T

18842525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117759698-G-A

18842525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117759698-G-T

18843192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117759992-G-T

18843329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117760097-G-A

18843570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117760353-T-C

18845339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117762293-T-C

18845404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117762350-T-A

18845404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117762350-T-C

18845734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117762638-A-G

http://identifiers.org/hco/16/GRCh38#18845790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117762699-C-A

18845790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117762699-C-G

18845790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117762699-C-T

18846054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117762858-T-G

18847593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117765333-C-T

18847752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117765450-T-C

18847752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117765450-T-G

18848044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117765815-A-T

http://identifiers.org/hco/16/GRCh38#18848110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117765858-A-C

18848110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117765858-A-G

18848111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117765859-T-C

http://identifiers.org/hco/16/GRCh38#18848176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117765894-A-C

18849269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117766397-C-T

18849299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117766427-A-G

18849408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117766520-T-C

http://identifiers.org/hco/16/GRCh38#18849483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117766584-A-C

18849698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117766785-T-C

18849768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117766857-T-G

18849803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117766896-T-A

18849803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117766896-T-C

18849803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117766896-T-G

18849814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117766907-G-A

18849814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117766907-G-T

18849818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117766911-G-C

18849818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117766911-G-T

18849839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117766931-G-T

18850022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117767109-G-A

18850022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117767109-G-C

http://identifiers.org/hco/16/GRCh38#18850055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117767142-A-C

18850493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117767573-C-T

http://identifiers.org/hco/16/GRCh38#18850509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117767582-C-A

18850536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117767605-G-A

18850536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117767605-G-T

18852273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117768032-T-C

http://identifiers.org/hco/16/GRCh38#18852305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117768064-C-A

18852305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117768064-C-T

18852610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117768360-G-T

http://identifiers.org/hco/16/GRCh38#18852612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117768362-C-A

18852612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117768362-C-T

http://identifiers.org/hco/16/GRCh38#18852778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117768522-A-C

18852787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117768531-G-A

18853652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: missense variant
orthologous variants: 117770978-T-C

18853683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: synonymous variant
orthologous variants: 117771009-T-C

18854530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117772192-A-G

18854564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117772226-G-T

18854602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117772261-C-T

http://identifiers.org/hco/16/GRCh38#18854945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117772566-A-C

18854945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117772566-A-G

18854956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117772578-C-T

http://identifiers.org/hco/16/GRCh38#18855032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117772615-C-A

18855777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117773402-T-C

18856087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117773680-C-T

18856890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117774029-G-A

http://identifiers.org/hco/16/GRCh38#18857043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117774145-C-A

http://identifiers.org/hco/16/GRCh38#18857243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117774313-C-A

18857243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117774313-C-T

http://identifiers.org/hco/16/GRCh38#18857417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117774492-C-A

18857697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117775496-C-G

18857697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117775496-C-T

18857777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117775580-G-A

18857777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117775580-G-C

18857777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117775580-G-T

http://identifiers.org/hco/16/GRCh38#18857959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117775761-C-A

18857962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117775765-A-G

18858002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117775793-G-C

18858002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117775793-G-T

18858038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117775813-G-A

18858038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117775813-G-C

18858038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117775813-G-T

18858203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117776094-T-C

18858592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117776711-G-A

18858855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117776878-A-G

18858855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117776878-A-T

18859085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117777651-A-G

18859303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117777863-G-C

http://identifiers.org/hco/16/GRCh38#18859362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117777919-C-A

18859362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117777919-C-T

18859388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117777925-T-A

18859388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117777925-T-C

18859732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117778152-G-T

18859843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117778252-G-A

18860396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117779303-C-G

http://identifiers.org/hco/16/GRCh38#18860545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117779451-C-A

18860545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117779451-C-T

18860608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117779515-G-C

18860608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117779515-G-T

http://identifiers.org/hco/16/GRCh38#18860825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117779756-C-A

18860825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117779756-C-G

18860825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117779756-C-T

18860959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117779862-A-G

18861007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117779922-T-C

18861043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117779957-T-C

18861092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117780001-G-A

18861092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117780001-G-T

18861449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117780401-G-A

18861619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117780638-G-A

18861619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117780638-G-T

http://identifiers.org/hco/16/GRCh38#18863474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117781469-A-C

18863626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117781573-A-G

18863626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117781573-A-T

18863638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117781585-A-G

18863677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: missense variant
orthologous variants: 117781624-T-A

18863677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: missense variant
orthologous variants: 117781624-T-C

18863844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: synonymous variant
orthologous variants: 117781791-G-T

18863871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117781831-T-G

18863906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117781878-T-G

18863921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117781897-A-G

18863921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117781897-A-T

http://identifiers.org/hco/16/GRCh38#18864123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117782088-C-A

18864123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: missense variant
orthologous variants: 117782088-C-G

18864123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: synonymous variant
orthologous variants: 117782088-C-T

http://identifiers.org/hco/16/GRCh38#18864135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117782100-C-A

18864135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: synonymous variant
orthologous variants: 117782100-C-T

18866384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 117782751-T-C

18866492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, missense_variant
orthologous variants: 117782856-G-A

18866492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, stop_gained
orthologous variants: 117782856-G-C

18866492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, stop_gained
orthologous variants: 117782856-G-T

http://identifiers.org/hco/16/GRCh38#18866529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117782887-C-A

18866529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117782887-C-T

18866607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117782948-T-C

18866887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117783222-T-A

18866887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117783222-T-C

18866901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117783236-T-C

18866927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117783257-A-G

18868199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 117783705-G-A

18868199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 117783705-G-T

18868208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 117783714-T-C

18868419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117783952-T-C

18868889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117784372-T-C

18868990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117784465-T-C

18869010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117784482-C-T

18869011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117784483-A-G

18869066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117784538-T-C

18869093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 117784566-G-C

18869228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 117784714-G-A

18869243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 117784729-C-T

18869550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117784963-T-G

http://identifiers.org/hco/16/GRCh38#18869585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#117784998-C-A

18869782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117785189-A-G

18869819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117785233-G-T

18870085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117785485-T-C

18870550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117788249-G-A

18870644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 117788328-G-A

18870644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 117788328-G-T

http://identifiers.org/hco/16/GRCh38#18870733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117788414-A-C

18870733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117788414-A-G

18870738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117788419-A-G

18870790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117788471-T-C

http://identifiers.org/hco/16/GRCh38#18870950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117788637-C-A

18870950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117788637-C-G

18871234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117788894-T-C

18871252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117788912-T-C

http://identifiers.org/hco/16/GRCh38#18871280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117788930-C-A

18871280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117788930-C-T

18871346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117788988-A-G

http://identifiers.org/hco/16/GRCh38#18871572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117789200-C-A

http://identifiers.org/hco/16/GRCh38#18871597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117789225-A-C

18871612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117789236-A-T

18871945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117789500-T-C

18872033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117789607-T-G

18872043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117789614-T-A

18872043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117789614-T-C

18872150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117789673-T-C

18872462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117789981-G-A

18872462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117789981-G-C

18872462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 117789981-G-T

18872513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 117790027-A-G

18872513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 117790027-A-T

18872698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117790212-A-G

18872722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117790237-A-T

http://identifiers.org/hco/16/GRCh38#18872772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117790301-A-C

18873711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117790657-G-A

18873711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117790657-G-T

18873718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117790666-G-A

18873893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117790818-T-C

18873996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117790924-A-G

18874515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117791110-A-G

18876071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117792636-T-C

18876071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117792636-T-G

18876116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 117792665-A-G

18876116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 117792665-A-T

18876235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117792784-T-G

18876524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793030-T-C

http://identifiers.org/hco/16/GRCh38#18876529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117793035-C-A

18876529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793035-C-T

18877017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117794165-A-G

18877158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117794286-T-C

18877158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117794286-T-G

http://identifiers.org/hco/16/GRCh38#18877206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117794334-C-A

18877206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117794334-C-T

18877286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117794413-G-A

18877286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117794413-G-C

18877286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117794413-G-T

18879816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117795356-T-C

http://identifiers.org/hco/16/GRCh38#18879819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117795359-C-A

18879819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117795359-C-T

18879820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117795360-T-A

18879894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117795550-T-C

18879933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117795591-T-G

18879994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117795647-A-G

18880174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117795833-C-G

18882042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117797321-A-T

http://identifiers.org/hco/16/GRCh38#18882047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117797326-C-A

18882047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117797326-C-T

http://identifiers.org/hco/16/GRCh38#18882089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117797363-C-A

18883062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117799069-T-C

18883112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117799120-G-A

18883494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117799453-T-G

18883568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117799524-G-A

18884094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: synonymous variant
orthologous variants: 117799908-C-T

18884194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117800018-A-G

18884194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117800018-A-T

18884198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117800022-T-A

18884198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117800022-T-C

18884198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117800022-T-G

http://identifiers.org/hco/16/GRCh38#18884213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117800037-C-A

18884213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117800037-C-T

http://identifiers.org/hco/16/GRCh38#18884215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117800039-C-A

18884283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117800069-C-T

18884640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117800451-G-A

18884735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117800513-A-G

18884757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117800529-C-T

18885205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117801877-A-G

18885264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117801933-G-C

18885268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117801937-T-C

18885268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117801937-T-G

18885325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117801973-C-T

http://identifiers.org/hco/16/GRCh38#18885337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117801986-C-A

18885337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117801986-C-T

18885449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117802161-T-A

18885449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117802161-T-C

18885993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117802546-C-T

http://identifiers.org/hco/16/GRCh38#18886005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117802554-A-C

18886048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117802595-T-C

18886048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117802595-T-G

18886164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117802695-G-C

18887188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117805052-T-C

18888368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117805779-A-G

18888392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117805803-G-A

http://identifiers.org/hco/16/GRCh38#18888446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117805857-A-C

18889655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117806309-T-C

18890682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117807111-T-C

18890730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117807150-A-G

18890749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117807169-T-C

18890780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117807177-G-T

18890998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117807372-T-A

http://identifiers.org/hco/16/GRCh38#18891005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117807379-C-A

18891005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117807379-C-T

http://identifiers.org/hco/16/GRCh38#18891315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117807746-C-A

18892175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117809919-G-A

18892188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117809933-T-G

18896330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117811893-T-C

18896495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117812007-T-C

http://identifiers.org/hco/16/GRCh38#18896703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117812055-A-C

18897032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117812354-T-A

18897032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117812354-T-C

18897045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117812367-A-G

18897830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117813920-A-G

18898072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117815129-T-C

http://identifiers.org/hco/16/GRCh38#18898291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117815276-C-A

18898445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117815446-C-T

18898628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117815653-T-C

18898644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117815679-T-C

18898662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117815697-T-C

18898840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117815847-T-C

http://identifiers.org/hco/16/GRCh38#18899234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117816219-C-A

http://identifiers.org/hco/16/GRCh38#18899277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117816262-C-A

18899315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117816301-C-T

18899720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117816682-G-A

18900083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117817039-G-A

18900083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117817039-G-C

18900173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117817125-T-A

18900189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117817141-G-A

18900189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117817141-G-T

http://identifiers.org/hco/16/GRCh38#18900198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117817150-C-A

http://identifiers.org/hco/16/GRCh38#18900336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117817287-A-C

18900454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117817392-C-G

18900500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117817446-T-C

18900824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117817704-C-G

18900824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117817704-C-T

18909644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117829622-T-C

18909775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117829742-C-G

18910003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117829952-G-A

18910023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117829965-T-C

18910684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117830058-T-C

18910975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117830279-A-G

18911022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117830317-T-C

http://identifiers.org/hco/16/GRCh38#18911709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117831329-C-A

18911709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 117831329-C-T

18911757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 117831369-T-A

18911757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 117831369-T-C

18914557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 117833084-G-A

18914818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 117833319-C-T

18914924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 117833428-G-T

18916636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117835126-G-A

18916696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117835172-G-A

18918339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117835819-C-G

18922185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117838657-T-C

18922203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117838673-T-C

http://identifiers.org/hco/16/GRCh38#18922209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117838679-C-A

http://identifiers.org/hco/16/GRCh38#18922425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#117838809-C-A

18923910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117840550-G-T

18923919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117840561-T-C

18924506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron variant
orthologous variants: 117841155-T-C

18925515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117842086-G-A

18925515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117842086-G-C

18925549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 117842120-G-A

18925549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 117842120-G-T

18925595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117842163-T-C

18925732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117842235-T-A

18925732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117842235-T-C

http://identifiers.org/hco/16/GRCh38#18925740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#117842244-C-A

18925740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117842244-C-G

18925740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117842244-C-T

18925770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117842270-T-C

18925770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117842270-T-G

18926213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117842655-G-A

18926213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117842655-G-C

18926213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117842655-G-T

18926351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117842793-G-A

18926351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117842793-G-T