111927174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5 prime UTR variant
orthologous variants: 50650756-G-T

111927177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5 prime UTR variant
orthologous variants: 50650753-T-A

111927177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5 prime UTR variant
orthologous variants: 50650753-T-C

111927206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 50650725-C-T

111927227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 50650704-G-A

111927227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 50650704-G-T

http://identifiers.org/hco/11/GRCh38#111927248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50650683-C-A

111927248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5 prime UTR variant
orthologous variants: 50650683-C-T

111927262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5 prime UTR variant
orthologous variants: 50650668-G-A

111927262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5 prime UTR variant
orthologous variants: 50650668-G-T

111927331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5 prime UTR variant
orthologous variants: 50650601-G-T

111927394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 50650557-G-A

111927394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 50650557-G-T

111927464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50650481-G-A

111927497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50650459-A-T

111927502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50650454-T-C

http://identifiers.org/hco/11/GRCh38#111927504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50650452-A-C

111927504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50650452-A-G

111927509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50650447-C-T

111927684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50650276-G-A

http://identifiers.org/hco/11/GRCh38#111928137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: -C-A

111929105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50649669-G-A

111929410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50649419-A-G

111929685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50649161-A-G

111929685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50649161-A-T

111929712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50649134-T-G

111929715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50649131-G-A

111929715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50649131-G-C

111929715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50649131-G-T

111929729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50649117-G-T

111929770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50649076-T-A

111929824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50649027-C-T

http://identifiers.org/hco/11/GRCh38#111929967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50648886-C-A

111929967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50648886-C-G

111930124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50648754-G-A

111931997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50646475-T-C

http://identifiers.org/hco/11/GRCh38#111932006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50646466-A-C

http://identifiers.org/hco/11/GRCh38#111932704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50646310-C-A

111932723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50646292-C-T

111933073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50645969-C-T

111933727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50643664-G-T

111934322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50643033-G-C

111934680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50642693-T-A

111934695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50642688-A-G

111935091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50642136-T-G

111935097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50642124-A-T

111935138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50642086-C-T

111935197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50642026-G-T

111935288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50641936-T-A

http://identifiers.org/hco/11/GRCh38#111935956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50640982-A-C

111936184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50640760-G-A

111936412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50640536-T-A

111936652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50639945-T-C

http://identifiers.org/hco/11/GRCh38#111936936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50639645-C-A

111936936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50639645-C-T

111937073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50639563-A-G

111937073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50639563-A-T

http://identifiers.org/hco/11/GRCh38#111937119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50639515-C-A

111937119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50639515-C-G

111937119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50639515-C-T

111937211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50639419-G-A

111937211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50639419-G-T

111937244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50639386-C-G

http://identifiers.org/hco/11/GRCh38#111937353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50639272-C-A

111937353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50639272-C-T

111937425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 50639200-G-A

111937425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 50639200-G-T

111937438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50639187-A-G

111937565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50639078-T-G

http://identifiers.org/hco/11/GRCh38#111937657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50639002-C-A

111937657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50639002-C-G

111937657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50639002-C-T

http://identifiers.org/hco/11/GRCh38#111937658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50639001-C-A

111937658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50639001-C-G

111937671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50638988-G-A

111937671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50638988-G-T

http://identifiers.org/hco/11/GRCh38#111937684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50638975-C-A

111937684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50638975-C-T

111937830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50638818-C-T

111938316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50638328-C-T

111938625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50637864-A-G

111938661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50637825-A-T

111938736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50637750-G-C

111938989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50637484-C-G

111938990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50637483-T-A

111939053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50637418-C-T

http://identifiers.org/hco/11/GRCh38#111939188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50637298-A-C

111939305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50637178-C-G

111940431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50636002-A-G

111940494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50635355-T-C

111940614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50635236-T-C

111940954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50634857-A-G

111941489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50634633-C-T

111941631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50634504-C-T

111941715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50634415-G-T

111941790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50634353-C-T

111942058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50634015-G-C

111942136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50633955-A-G

111942275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50633810-G-A

111942600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50633470-T-C

111944282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50632752-T-C

111944705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50632292-G-A

111944705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50632292-G-T

111947303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50630410-A-G

111947332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50630376-T-C

111947360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50630348-T-C

111947383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50630326-T-C

111947581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50629882-T-G

111947684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50629772-A-G

111947732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50629725-C-G

http://identifiers.org/hco/11/GRCh38#111947769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50629686-A-C

111948298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50629190-A-G

111948327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50629161-C-T

111948457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50629042-C-T

111948552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50628958-T-A

111961136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50626430-G-A

111961137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50626429-G-A

111961324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50626255-T-A

111961327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50626252-T-C

111961475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50626107-T-A

111961614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50625969-G-A

111961614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50625969-G-C

111961822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50625763-A-G

111961873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50625712-A-G

111961951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50625652-G-A

111961996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50625607-C-G

111962513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50624624-A-G

111962651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50624469-A-G

111962671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50624450-A-G

111962671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50624450-A-T

111962885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50624175-G-A

http://identifiers.org/hco/11/GRCh38#111962902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50624171-C-A

111962902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50624171-C-T

111963376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50623347-G-A

111963570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50623170-G-A

111963788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50622972-C-T

111963886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50622873-T-C

111963920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50622839-C-T

111964051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50622710-G-A

111964314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50622481-C-T

111965320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50621295-A-G

111965515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50621133-A-G

http://identifiers.org/hco/11/GRCh38#111965734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50620958-A-C

http://identifiers.org/hco/11/GRCh38#111965764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50620926-A-C

111965766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50620924-G-A

111968437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50617634-T-C

111968464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50617608-T-A

http://identifiers.org/hco/11/GRCh38#111968653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50617393-A-C

111968656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50617368-T-A

111969566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50616403-C-G

111969566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50616403-C-T

111969683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50616307-T-G

111972172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50616148-T-G

111972253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50616070-C-T

111973518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50615113-T-G

111973572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50615060-G-A

http://identifiers.org/hco/11/GRCh38#111973878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50614777-C-A

111973878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50614777-C-T

111973906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50614751-G-T

111973931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50614727-A-G

111973950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50614708-A-G

111973960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50614698-A-T

111973998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50614660-A-G

111973998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50614660-A-T

111974073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50614601-G-T

111974088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50614586-C-G

111974267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 50614413-A-G

http://identifiers.org/hco/11/GRCh38#111974373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50614305-A-C

111974373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50614305-A-G

111974373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50614305-A-T

111974376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50614302-G-T

111974452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50614003-T-A

http://identifiers.org/hco/11/GRCh38#111974455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50614000-C-A

111974455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50614000-C-T

http://identifiers.org/hco/11/GRCh38#111974755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50613728-A-C

111974755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50613728-A-G

111974779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50613585-G-A

111975033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50613150-G-A

111975152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50612470-G-A

111975152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50612470-G-T

111975174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50612456-G-A

111975213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50612417-G-C

111975242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 50612388-G-A

111975312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50612322-G-T

http://identifiers.org/hco/11/GRCh38#111975414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50612214-C-A

111975580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50612045-T-A

111975675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50611942-T-C

111975765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50611855-T-C

111975776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50611844-T-C

111975777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50611843-G-C

111975777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50611843-G-T

111975873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50611744-T-C

111975900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50611717-C-G

111975914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 50611703-T-G

http://identifiers.org/hco/11/GRCh38#111976073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50611558-C-A

111976367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50611276-C-T

http://identifiers.org/hco/11/GRCh38#111976801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50610906-C-A

111976823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50610884-T-C

111976940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50610707-A-G

111976958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 50610677-C-T

http://identifiers.org/hco/11/GRCh38#111976963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50610672-C-A

http://identifiers.org/hco/11/GRCh38#111977044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50610573-C-A

111977100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50610522-G-A

111977109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50610513-A-G

http://identifiers.org/hco/11/GRCh38#111977187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50610462-C-A

111977187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50610462-C-G

111977212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50610436-G-A

111977212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50610436-G-T

http://identifiers.org/hco/11/GRCh38#111977277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50610381-C-A

111977277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50610381-C-G

111977277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50610381-C-T

111977290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50610367-G-C

111977416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50610234-G-A

111977416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50610234-G-C

111977455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 50610195-G-A

111977455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 50610195-G-T

111977456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 50610194-C-T

111977461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 50610189-G-C

111977461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 50610189-G-T

http://identifiers.org/hco/11/GRCh38#111977505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50610145-C-A

111977505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50610145-C-T

111977506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50610144-C-T

111977569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50610080-C-T

111977669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 50609981-C-G

111977694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 50609955-T-A

111977817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50609833-T-A

111977817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50609833-T-G

111977874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50609777-G-A

111978115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50609554-A-G

111978124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50609545-T-C

111978572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50609143-C-T

111978635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50609076-C-T

111979233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50608521-C-T

http://identifiers.org/hco/11/GRCh38#111979303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50608465-A-C

111979391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50608373-T-A

111979457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50608307-C-T

111979485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50608279-T-A

http://identifiers.org/hco/11/GRCh38#111980452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50607457-C-A

111980463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50607446-T-G

111980670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50606946-T-A

111980688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50606928-G-T

111980745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 50606873-C-T

http://identifiers.org/hco/11/GRCh38#111980864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50606762-C-A

111980864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50606762-C-G

http://identifiers.org/hco/11/GRCh38#111980940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50606685-C-A

111980940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50606685-C-T

111980976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50606649-T-A

111980976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50606649-T-C

http://identifiers.org/hco/11/GRCh38#111981039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50606586-A-C

http://identifiers.org/hco/11/GRCh38#111981516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50606123-A-C

111981528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50606111-T-C

111981689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron variant
orthologous variants: 50605894-T-G

111982098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50605228-T-G

http://identifiers.org/hco/11/GRCh38#111982109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50605217-A-C

111982109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50605217-A-G

http://identifiers.org/hco/11/GRCh38#111982126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50605203-A-C

111982126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, undefined
orthologous variants: 50605203-A-G

111982278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 50605047-G-A

111982278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 50605047-G-T

111982280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 50605045-T-G

111982338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: non_coding_transcript_exon_variant, splice_acceptor_variant
orthologous variants: 50604990-G-A

111982355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 50604973-A-G

http://identifiers.org/hco/11/GRCh38#111982371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50604957-C-A

111982371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50604957-C-T

111982510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50604818-G-T

111982547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50604775-T-C

111983004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50604430-A-G

111983133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50604297-G-C

111983303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50604120-C-T

111983390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50604037-A-G

111983609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50603832-A-G

111984042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50603394-G-A

111984709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50601924-A-G

111984916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50601726-T-C

111985000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 50601651-G-A

111985183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50601297-A-T

111985238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 50601241-C-T

111985253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 50601226-T-C

111985328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 50601151-T-C

111985372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50601148-G-A

http://identifiers.org/hco/11/GRCh38#111985944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50600603-C-A

111985944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50600603-C-G

http://identifiers.org/hco/11/GRCh38#111986119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50600478-C-A

111986474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50600186-C-T

111986613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50600147-C-T

111986615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50600145-C-T

111986669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50600105-A-G

111986748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50600043-C-T

http://identifiers.org/hco/11/GRCh38#111986775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50600033-C-A

111986775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50600033-C-T

http://identifiers.org/hco/11/GRCh38#111986782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50600026-C-A

111986812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50599996-G-C

111986969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50599855-G-A

111986969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50599855-G-T

111988403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50599285-T-C

111988849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50598864-A-G

111989039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50598675-A-G

111989112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50598568-G-A

111989112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50598568-G-C

111989112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50598568-G-T

111989120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50598560-G-T

111989123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50598557-G-T

111989186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50598473-G-T

111991190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50597463-A-G

111991191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50597462-A-G

111991224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50597429-G-A

111991352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50597088-T-C

111991364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50597076-T-C

111991374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50597067-A-G

111991426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50597021-G-A

111991426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50597021-G-T

111991955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50596659-C-T

111992128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50596508-C-T

111992287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50596343-T-C

111992287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50596343-T-G

111992365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50596276-G-T

111992373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50596268-G-A

111992373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50596268-G-T

http://identifiers.org/hco/11/GRCh38#111992439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50596206-C-A

111992439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 50596206-C-T

111992472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 50596173-G-T

111992528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50596117-A-G

111992588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50596059-T-A

111992588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50596059-T-G

http://identifiers.org/hco/11/GRCh38#111992666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50595980-A-C

111992666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595980-A-G

111992804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595849-G-T

111992859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595794-A-G

http://identifiers.org/hco/11/GRCh38#111992879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50595778-A-C

111992907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595750-G-A

111992907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595750-G-T

111992922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595735-G-A

111992972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50595684-G-A

111992972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50595684-G-T

111993016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595643-T-C

111993067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595601-T-C

111993077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595591-A-G

111993078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595590-G-A

111993082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595586-T-C

111993118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595571-T-A

111993124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595565-T-C

111993209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595496-G-A

111993437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595322-G-C

111993437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595322-G-T

111993463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595296-G-T

111993568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50595192-T-A

111993595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 50595165-A-T

111993609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595152-T-C

111993651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595109-T-A

111993651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50595109-T-G

111993789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50594994-G-A

http://identifiers.org/hco/11/GRCh38#111993801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50594985-C-A

111993850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50594928-A-G

111993945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50594893-T-A

111994475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50594567-A-G

111994475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50594567-A-T

111994490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50594552-C-T

111994496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50594546-T-C

111994516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50594526-T-C

111994566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50594481-T-C

111994636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50594421-A-G

111995048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 50593895-A-G

111995071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50593872-C-T

111995187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50593766-G-A

111995187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50593766-G-T

111995201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50593753-T-G

http://identifiers.org/hco/11/GRCh38#111995279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50593650-C-A

111995279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50593650-C-T

111995524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50593371-G-A

111995524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 50593371-G-T

111995661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50593252-A-G

111995740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50593185-A-G

111995889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50593035-G-A

111996061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50592870-T-C

http://identifiers.org/hco/11/GRCh38#111996089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50592842-A-C

111996166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50592765-C-T

111996173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50592758-G-A

111996173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50592758-G-T

111996243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50590695-A-G

111996289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50590649-T-G

111996327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50590608-C-T

http://identifiers.org/hco/11/GRCh38#111996401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50590554-A-C

111998931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50587629-G-A

111999080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50587493-G-A

112016595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50580944-T-A

112016595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50580944-T-C

112016635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50580904-A-G

112016635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50580904-A-T

112016837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50580709-A-G

112017027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50580161-C-G

http://identifiers.org/hco/11/GRCh38#112017032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50580156-A-C

112017096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50580110-T-C

112017123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50580082-G-C

112017318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50579840-T-G

112017469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50579351-T-C

http://identifiers.org/hco/11/GRCh38#112017597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50579246-C-A

112017597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50579246-C-G

http://identifiers.org/hco/11/GRCh38#112017647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50579203-C-A

112017647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50579203-C-T

http://identifiers.org/hco/11/GRCh38#112017652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50579197-C-A

112017652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50579197-C-T

112017735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50579107-T-G

112017904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50578939-G-A

112017913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50578931-G-A

112019136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50577417-T-C

112019147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50577405-A-G

http://identifiers.org/hco/11/GRCh38#112019163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50577390-A-C

112019191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50577362-T-C

112019216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50577337-T-C

112019220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50577333-A-G

http://identifiers.org/hco/11/GRCh38#112019227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50577325-C-A

112019227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50577325-C-G

112019262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50577289-G-T

http://identifiers.org/hco/11/GRCh38#112019425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50577148-C-A

112019613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50576969-G-A

http://identifiers.org/hco/11/GRCh38#112019669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50576925-C-A

112019669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50576925-C-G

112019669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50576925-C-T

http://identifiers.org/hco/11/GRCh38#112020020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50576620-C-A

112020104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50576537-G-A

112020145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50576507-T-C

http://identifiers.org/hco/11/GRCh38#112020358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50576306-C-A

112020358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50576306-C-T

112020562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50576111-T-G

http://identifiers.org/hco/11/GRCh38#112020947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50575725-C-A

112021024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 50575648-T-G

112021088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3 prime UTR variant
orthologous variants: 50575596-C-T

112021239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3 prime UTR variant
orthologous variants: 50575440-G-T

http://identifiers.org/hco/11/GRCh38#112021335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50575365-A-C

112021341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3 prime UTR variant
orthologous variants: 50575360-A-G

112021690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3 prime UTR variant
orthologous variants: 50574972-T-C

112021712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3 prime UTR variant
orthologous variants: 50574952-T-C

112022009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3 prime UTR variant
orthologous variants: 50574690-A-T

112022161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3 prime UTR variant
orthologous variants: 50574444-G-T

112022648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3 prime UTR variant
orthologous variants: 50573986-G-A

112022648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23695
most severe consequence: 3 prime UTR variant
orthologous variants: 50573986-G-T