108942788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 56812348-G-A

108942860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, missense_variant
orthologous variants: 56812417-T-A

108942860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 56812417-T-C

108943171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron variant
orthologous variants: 56812682-G-T

108943218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron variant
orthologous variants: 56812727-G-A

http://identifiers.org/hco/9/GRCh38#108943678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56813133-A-C

http://identifiers.org/hco/9/GRCh38#108943680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56813135-A-C

108943680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron variant
orthologous variants: 56813135-A-G

108943687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron variant
orthologous variants: 56813142-C-T

108943688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron variant
orthologous variants: 56813143-A-G

108943766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 56813241-A-T

108944057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron variant
orthologous variants: 56813925-T-C

108944120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron variant
orthologous variants: 56813980-G-A

108944120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron variant
orthologous variants: 56813980-G-T

http://identifiers.org/hco/9/GRCh38#108944153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56814012-A-C

108944166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron variant
orthologous variants: 56814028-A-G

108944182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron variant
orthologous variants: 56814042-G-A

108948327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56816333-A-T

108948472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56816464-T-C

108948735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56816680-C-T

108952447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56817250-A-G

108952571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56817359-G-T

108952646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56817439-C-T

108953020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56817755-T-C

108953210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56817940-G-A

108953371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56818087-T-A

108953371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56818087-T-C

108953454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56818174-C-T

108953509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56818246-A-G

108955664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56822405-T-C

108955733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56822462-G-A

108955733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56822462-G-T

108955757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56822486-A-G

108955781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56822509-T-C

108955814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56822542-G-T

108955821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56822549-T-C

http://identifiers.org/hco/9/GRCh38#108955952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56822668-C-A

108956121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56822825-T-G

108956155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56822855-C-T

108956171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56822871-T-C

108961823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56824676-C-T

108961842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56824694-T-G

108962124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56824925-G-C

108962271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825078-A-G

108962285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825096-G-T

108962289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825100-A-G

108962317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825129-T-A

108962331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825143-C-T

http://identifiers.org/hco/9/GRCh38#108963272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56825285-C-A

108963322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825334-G-T

108963362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825390-A-G

http://identifiers.org/hco/9/GRCh38#108963388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56825432-C-A

108963389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825433-T-C

108964466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825666-C-G

108964666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56825862-C-T

108970243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827091-A-G

108970307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827164-A-G

108970307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827164-A-T

108970375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827226-A-G

108970375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827226-A-T

http://identifiers.org/hco/9/GRCh38#108970435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56827285-A-C

108970435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56827285-A-G

108970435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56827285-A-T

108970473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56827323-T-C

108970505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827354-A-G

108970506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827355-T-C

http://identifiers.org/hco/9/GRCh38#108970526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56827375-C-A

108970563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827405-T-A

108970563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827405-T-C

http://identifiers.org/hco/9/GRCh38#108970892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56827605-C-A

108970892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827605-C-T

108971042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56827784-G-T

108972237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829096-C-T

108972507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829311-C-T

108972573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829380-G-A

108972573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829380-G-T

http://identifiers.org/hco/9/GRCh38#108972672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56829481-C-A

108972728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56829537-C-G

108972814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56829623-T-A

108972814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56829623-T-C

http://identifiers.org/hco/9/GRCh38#108972966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56829739-C-A

108972966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829739-C-G

108972966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829739-C-T

108972968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829741-G-A

108972968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829741-G-T

108973042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829795-T-C

108973123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829828-T-G

108973192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56829893-C-G

108973853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56830874-C-T

108974018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56831022-G-A

108974052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56831044-A-T

108974134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56831150-T-A

108974134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56831150-T-C

108974260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56831234-T-A

108975851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56832185-C-T

108975902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56832237-C-T

108976303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56832629-A-G

108976424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56832697-A-T

http://identifiers.org/hco/9/GRCh38#108977075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56833018-A-C

108977075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56833018-A-G

108977096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56833038-T-C

108977182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56833143-T-C

108977270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56833243-A-T

108977389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56833348-A-T

http://identifiers.org/hco/9/GRCh38#108977451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56833598-A-C

108977733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56833784-T-C

108977835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56833872-C-T

108978008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834024-C-T

108978022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834038-T-A

108978462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834453-G-C

108978494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834485-T-C

108978700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834657-G-A

http://identifiers.org/hco/9/GRCh38#108978701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56834658-C-A

108978742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834697-C-G

http://identifiers.org/hco/9/GRCh38#108978766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56834717-A-C

108978774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834725-C-G

108978965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834904-T-G

108978975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56834914-G-A

108979130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835044-G-A

108979130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835044-G-T

108979167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835082-T-A

108979215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835114-A-G

108979260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835160-G-A

108979260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835160-G-T

108979265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835162-T-A

108979265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835162-T-C

108979422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56835319-C-T

108979595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835463-G-A

108979595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835463-G-T

108979605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835473-A-G

108979605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835473-A-T

108979606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835474-A-G

108979611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835479-G-A

108979752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835618-G-A

http://identifiers.org/hco/9/GRCh38#108979753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56835619-C-A

108979796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56835664-G-A

108980905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56836062-T-A

108980905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56836062-T-C

108980971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56836131-C-G

108981722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56836233-C-T

http://identifiers.org/hco/9/GRCh38#108981956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56836588-C-A

108981956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56836588-C-G

http://identifiers.org/hco/9/GRCh38#108982204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56836770-A-C

http://identifiers.org/hco/9/GRCh38#108982263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56836826-A-C

108982267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56836830-T-A

108983206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56837793-T-C

http://identifiers.org/hco/9/GRCh38#108983392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56837979-C-A

108983407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56837995-G-A

108983407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56837995-G-C

http://identifiers.org/hco/9/GRCh38#108983423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56838011-C-A

http://identifiers.org/hco/9/GRCh38#108983444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56838032-C-A

108983444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56838032-C-T

108983525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56838111-C-T

108983731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56838331-T-C

108983763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56838349-T-A

108983766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56838352-T-C

108983815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56838402-G-A

108983910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56838484-T-C

108983946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56838521-G-C

108983951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56838526-A-G

108983965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56838540-C-T

108984088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56838650-C-T

108984130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56838694-G-A

108984130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56838694-G-T

108984359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56838978-G-A

108984359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56838978-G-T

108984395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56839014-A-G

108984460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56839079-A-G

108984460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56839079-A-T

108984489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56839108-T-C

108988967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

108989135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56840449-C-T

http://identifiers.org/hco/9/GRCh38#108990613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56841449-C-A

108990613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56841449-C-T

108990662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56841497-T-C

108990667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56841502-C-T

http://identifiers.org/hco/9/GRCh38#108990668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56841503-C-A

108990668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56841503-C-T

108990726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 56841561-A-G

108990916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56841748-G-T

108991844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56843460-T-C

http://identifiers.org/hco/9/GRCh38#108991871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56843478-C-A

108991885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56843491-T-C

108991924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56843517-T-C

108991929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56843522-T-C

108991946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56843539-G-C

108991946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56843539-G-T

108991987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56843580-C-G

108991993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56843586-A-G

108992012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56843605-G-A

108992012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56843605-G-C

108992012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56843605-G-T

108992013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56843606-G-A

108992013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56843606-G-T

108992043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56843828-G-T

108992076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56843861-G-A

108992081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56843866-G-A

108992097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56843882-G-C

108992097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56843882-G-T

108992138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56843916-T-C

http://identifiers.org/hco/9/GRCh38#108992588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56844413-A-C

108992588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56844413-A-G

108992857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56844674-T-C

http://identifiers.org/hco/9/GRCh38#108992870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56844692-C-A

108992908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56844713-G-A

108992908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56844713-G-T

http://identifiers.org/hco/9/GRCh38#108992917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56844722-C-A

http://identifiers.org/hco/9/GRCh38#108992957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56844758-C-A

108992957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56844758-C-T

108993088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56844892-C-G

108993113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56844916-T-C

http://identifiers.org/hco/9/GRCh38#108993152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56844954-A-C

108996528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56846069-C-T

108996936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56846432-G-T

108997170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56846661-T-C

108997216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56846695-T-A

108997216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56846695-T-C

108997268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56846747-C-T

108998920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56846969-T-A

http://identifiers.org/hco/9/GRCh38#108998939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56846988-C-A

108999125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56847868-A-G

108999263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56848006-A-G

108999266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848009-A-T

108999304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848080-T-C

108999612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848351-T-C

108999683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848413-T-C

108999829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56848800-T-C

http://identifiers.org/hco/9/GRCh38#109005229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56856147-C-A

109005266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856184-A-G

109005408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856253-T-A

109005412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856256-A-G

109005491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856310-T-G

109005619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856434-C-T

109005650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856464-A-G

109005702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856583-T-C

109005743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856619-T-G

109005866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856741-G-T

109005933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56856807-T-C

109006279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56857879-C-T

109006427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56858028-C-T

109006520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56858109-G-A

109006544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56858133-A-G

109006713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56858294-G-A

http://identifiers.org/hco/9/GRCh38#109006823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56858395-A-C

109006833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56858405-G-T

109007126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56858731-T-C

109007191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56858838-C-T

109007192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56858839-G-A

109007263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56858953-G-A

109007344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56859035-A-G

109007356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56859047-A-G

109007442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56859130-G-A

109007583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56859249-A-T

109010358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56861543-T-C

109010358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56861543-T-G

109010382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56861567-C-T

109010465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56861647-G-A

http://identifiers.org/hco/9/GRCh38#109010677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56862012-C-A

109010988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56862310-C-T

109011018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56862331-G-C

109011340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863107-G-C

109011374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863141-A-G

http://identifiers.org/hco/9/GRCh38#109011472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56863219-C-A

109011504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863255-C-G

109011698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863462-C-T

109011951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56863686-G-C

http://identifiers.org/hco/9/GRCh38#109013185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56864864-C-A

109013185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56864864-C-T

109013187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56864866-G-A

109013187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56864866-G-T

109013379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56865054-A-G

http://identifiers.org/hco/9/GRCh38#109013458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2512
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#56865130-C-A