96281005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105579586-G-T

96281007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105579588-C-G

96281163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105579725-A-G

96281491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105579984-T-A

96281491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105579984-T-C

96281509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105580001-G-A

http://identifiers.org/hco/14/GRCh38#96281564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105580050-C-A

96281746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 105580173-G-C

96281746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 105580173-G-T

96281786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105580202-G-T

96282078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105580482-G-A

http://identifiers.org/hco/14/GRCh38#96282119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105580522-C-A

96282119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105580522-C-T

96282263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105580671-G-A

96283058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105580922-G-T

96283176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581011-T-A

96283176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581011-T-C

96283233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581051-G-A

96283233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581051-G-T

96283235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581053-G-T

96283349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581142-T-C

http://identifiers.org/hco/14/GRCh38#96283426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105581210-C-A

96283426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581210-C-T

96283434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581218-T-C

http://identifiers.org/hco/14/GRCh38#96283493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105581265-C-A

http://identifiers.org/hco/14/GRCh38#96283501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105581273-C-A

96283614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581389-T-C

96283634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581409-A-G

96283716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581485-A-G

96283736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581505-T-C

96283879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581576-G-A

96283879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581576-G-T

http://identifiers.org/hco/14/GRCh38#96284098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105581745-C-A

96284098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581745-C-G

96284215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581820-G-A

96284317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581942-C-G

96284317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581942-C-T

96284318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581943-T-A

96284318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581943-T-C

96284318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581943-T-G

96284333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105581960-T-C

http://identifiers.org/hco/14/GRCh38#96284338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105581965-C-A

96284437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105582129-G-T

96284494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105582184-G-A

http://identifiers.org/hco/14/GRCh38#96284507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105582196-C-A

96284648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105582300-T-G

96284701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105582350-T-C

http://identifiers.org/hco/14/GRCh38#96284713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105582362-A-C

96284920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105582563-G-T

96284935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105582575-G-A

http://identifiers.org/hco/14/GRCh38#96285031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105582673-C-A

96285031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105582673-C-G

96285031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105582673-C-T

96285139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105582778-A-G

http://identifiers.org/hco/14/GRCh38#96285316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105582900-C-A

96285316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105582900-C-T

http://identifiers.org/hco/14/GRCh38#96285383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105582974-C-A

96285383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105582974-C-G

http://identifiers.org/hco/14/GRCh38#96285484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105583078-C-A

96285531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105583120-G-A

96285538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105583124-G-C

96285541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3 prime UTR variant
orthologous variants: 105583127-A-G

http://identifiers.org/hco/14/GRCh38#96285690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#105583269-C-A

96285851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous_variant, undefined
orthologous variants: 105583428-T-C

96285851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous_variant, undefined
orthologous variants: 105583428-T-G

96286035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105583603-G-T

http://identifiers.org/hco/14/GRCh38#96286066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105583628-C-A

96286066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105583628-C-T

http://identifiers.org/hco/14/GRCh38#96286086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105583650-C-A

http://identifiers.org/hco/14/GRCh38#96286513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105584056-A-C

96288728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105584958-A-T

http://identifiers.org/hco/14/GRCh38#96288803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105585044-C-A

96288803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105585044-C-G

96289065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105585343-A-G

96289253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105586758-C-T

96289279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105586784-T-C

96289360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105586856-T-A

96289360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105586856-T-C

96289360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105586856-T-G

http://identifiers.org/hco/14/GRCh38#96289361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105586857-A-C

96289361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105586857-A-G

96289361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105586857-A-T

96289391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105586882-T-A

96289391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105586882-T-C

96289391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105586882-T-G

96289450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105586921-T-C

96289570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105587007-A-T

96289613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105587422-C-G

96289613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105587422-C-T

96289903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105587734-G-A

96289907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105587738-C-T

96289934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105587768-G-T

96289996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105587832-A-G

96290080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105587909-T-C

96290127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105587956-T-C

96290132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105587961-C-T

http://identifiers.org/hco/14/GRCh38#96290153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105587979-C-A

96290153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105587979-C-T

96290241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105588059-G-A

96290241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105588059-G-C

96290241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105588059-G-T

http://identifiers.org/hco/14/GRCh38#96290338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105588268-C-A

96290338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105588268-C-T

96290360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105588290-T-C

96290409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105588339-A-G

96290511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105588437-T-G

96290977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105589125-T-C

96291009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105589149-T-C

96291012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105589152-A-T

96291650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105589730-A-G

96291695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105589775-A-G

96291727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105589805-A-T

96291801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105589879-T-C

96291801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105589879-T-G

96291816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105589893-T-A

96291816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105589893-T-C

96291824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105589901-T-C

96291824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105589901-T-G

96291834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105589919-T-C

96291834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105589919-T-G

96291848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105589933-T-A

96291848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105589933-T-C

96291848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105589933-T-G

96291897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105590018-T-C

http://identifiers.org/hco/14/GRCh38#96291910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105590031-C-A

96291910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105590031-C-T

96291914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105590035-G-T

96291997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105590142-T-C

96292004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105590149-G-C

96292004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105590149-G-T

96292178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105590303-T-C

96292181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105590306-G-A

96292181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105590306-G-T

http://identifiers.org/hco/14/GRCh38#96292283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105590408-C-A

96292283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105590408-C-T

96292354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105590485-T-C

96292661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105590752-A-G

http://identifiers.org/hco/14/GRCh38#96292680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105590769-C-A

http://identifiers.org/hco/14/GRCh38#96292744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105590828-C-A

96292744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105590828-C-T

http://identifiers.org/hco/14/GRCh38#96293346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105591060-C-A

96293652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105591247-G-T

96293694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105591289-G-A

96293820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105591448-G-A

96293914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105591599-T-C

96293941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105591626-A-T

96293988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105591672-C-T

96294132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105591811-G-A

96294132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105591811-G-C

96294212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105591869-G-C

96294427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592025-C-G

96294427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592025-C-T

96294438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592036-G-A

http://identifiers.org/hco/14/GRCh38#96294455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105592045-C-A

96294455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592045-C-T

96294637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592178-T-C

96294668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592215-A-G

96294668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592215-A-T

96294797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592291-G-T

96294823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592313-G-T

http://identifiers.org/hco/14/GRCh38#96294868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105592343-C-A

96294868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592343-C-T

http://identifiers.org/hco/14/GRCh38#96294890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105592365-C-A

96294890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592365-C-T

96294999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105592476-G-A

http://identifiers.org/hco/14/GRCh38#96295031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105592505-C-A

96295090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105592564-T-C

96295090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105592564-T-G

96295208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592678-T-G

96295214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592684-T-A

96295214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592684-T-C

96295216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592686-G-A

96295216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592686-G-T

96295458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592962-T-C

96295558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 105593063-A-T

http://identifiers.org/hco/14/GRCh38#96295643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105593135-A-C

96295643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105593135-A-G

96295670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105593158-G-T

http://identifiers.org/hco/14/GRCh38#96295762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105593239-C-A

96295762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105593239-C-T

96298516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105598418-C-T

96298569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105598454-T-C

96298666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105598513-G-C

96298683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105598528-T-A

96298836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105598637-A-G

96298939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105598731-A-T

96298990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105598795-A-G

96299054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105598855-C-T

96299309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105599172-A-G

96300740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105600307-T-C

96301198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105600727-T-G

96301862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601054-G-A

96301862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601054-G-C

96301868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601060-G-T

96301926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601079-T-A

96302121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601288-A-G

96302211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601375-A-G

http://identifiers.org/hco/14/GRCh38#96303038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105601917-A-C

96303038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601917-A-T

http://identifiers.org/hco/14/GRCh38#96304377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105602608-C-A

96304377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105602608-C-T

96304430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105602654-G-A

96304430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105602654-G-T

http://identifiers.org/hco/14/GRCh38#96304435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105602659-C-A

96304435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105602659-C-G

96304486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105602697-C-T

96304585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105602796-A-G

96304585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105602796-A-T

http://identifiers.org/hco/14/GRCh38#96304610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105602821-A-C

96304610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105602821-A-T

96304635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105602848-T-C

96304635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105602848-T-G

96305304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105603725-A-G

http://identifiers.org/hco/14/GRCh38#96305900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105604454-C-A

96305900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105604454-C-T

96305952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105604594-G-A

96305957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105604599-T-A

96305957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105604599-T-C

96305957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105604599-T-G

96306585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605359-T-A

96306585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605359-T-C

96306585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605359-T-G

96306609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605381-G-A

96306609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605381-G-C

96306609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605381-G-T

96306616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605388-A-G

96306698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605445-G-A

96306698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605445-G-C

96306756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105605503-A-G

96306952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605698-G-A

96306952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605698-G-C

96306952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605698-G-T

http://identifiers.org/hco/14/GRCh38#96306960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105605706-A-C

http://identifiers.org/hco/14/GRCh38#96307046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105605816-A-C

96307046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605816-A-G

96307046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605816-A-T

96307059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605829-T-A

96307059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605829-T-C

96309353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105607317-T-C

96309476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105607434-G-A

96309479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105607437-G-C

96309498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105607456-T-A

96309544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105607502-T-G

96309583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105607541-A-G

96309593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 105607551-A-G

96309603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105607560-A-T

96309621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105607578-T-A

96310096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105608647-C-T

96310149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105608697-G-A

http://identifiers.org/hco/14/GRCh38#96310346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105608858-C-A

96310346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105608858-C-T

96310492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105609007-T-C

96310677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105609181-A-G

96310734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105609213-T-C

96310755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105609235-C-G

96310755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105609235-C-T

96310785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105609262-T-C

96310795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105609272-A-T

96310925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105609342-T-C

96311166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105609498-G-A

96311195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105609527-C-T

http://identifiers.org/hco/14/GRCh38#96311219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105609551-A-C

96311320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105609652-T-C

96311500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105610009-A-G

http://identifiers.org/hco/14/GRCh38#96311657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105610159-C-A

96311657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105610159-C-T

96311740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105610232-T-A

96311740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105610232-T-C

96311740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105610232-T-G

http://identifiers.org/hco/14/GRCh38#96311745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105610241-C-A

96312062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105610525-C-T

96313139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105611165-G-T

96313162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 105611188-T-C

96313162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 105611188-T-G

96313169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105611195-G-T

96313196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105611222-C-G

96313196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105611222-C-T

96313197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105611223-G-A

96313197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105611223-G-T

96313219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105611246-A-T

96313257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105611320-G-T

96313301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105611606-C-T

http://identifiers.org/hco/14/GRCh38#96313462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105611762-C-A

96313509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105611808-T-A

96313509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105611808-T-C

96313509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105611808-T-G

96315123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105612754-T-G

96315190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105612819-A-G

96315211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105612840-C-T

96315247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105612879-A-T

http://identifiers.org/hco/14/GRCh38#96315289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105612917-A-C

96315300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105612926-C-G

96315596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105613222-A-G

http://identifiers.org/hco/14/GRCh38#96315714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105614130-A-C

96315767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105614181-C-T

96315791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105614220-G-T

96316396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105614444-A-G

96316405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105614453-G-A

96316405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105614453-G-T

http://identifiers.org/hco/14/GRCh38#96316492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105614535-C-A

96316492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105614535-C-G

96316540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: stop gained
orthologous variants: 105614579-G-T

96316615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105614654-T-C

96316741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105614888-T-C

96316901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105615043-G-C

96317007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105615167-T-C

http://identifiers.org/hco/14/GRCh38#96317071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105615224-C-A

96317071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105615224-C-T

96317552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615629-G-A

http://identifiers.org/hco/14/GRCh38#96317560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105615635-C-A

96317726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105615762-A-G

96317867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615906-A-G

96317877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615916-A-G

96317931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615954-T-A

96317949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615972-A-G

96317994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105616014-T-C

http://identifiers.org/hco/14/GRCh38#96318121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105616106-C-A

96318122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105616107-T-G

http://identifiers.org/hco/14/GRCh38#96322107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105617635-C-A

96322223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105617751-G-A

96322320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105617856-T-C

http://identifiers.org/hco/14/GRCh38#96322494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105618175-C-A

96322582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105618360-T-C

96323973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105618865-A-G

96323973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105618865-A-T

96324040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105618930-A-G

96324129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105618981-G-A

96324129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 105618981-G-T

96324232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105619071-A-G

96324243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105619080-T-A

96324243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105619080-T-C

http://identifiers.org/hco/14/GRCh38#96324249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105619086-A-C

96324253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105619090-A-G

96324278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105619112-G-T

96324287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105619121-G-T

96325515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105620155-T-C

http://identifiers.org/hco/14/GRCh38#96325518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105620158-C-A

96325518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105620158-C-T

96325537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105620162-G-A

96325537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105620162-G-T

96325633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105620252-G-A

96326007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105620582-A-G

http://identifiers.org/hco/14/GRCh38#96326065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105620632-C-A

96326065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105620632-C-T

96326215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105620757-C-T

96326226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105620767-T-A

96328318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105624198-A-G

96328322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105624202-G-A

96328322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105624202-G-T

http://identifiers.org/hco/14/GRCh38#96328371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105624250-A-C

96328371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105624250-A-G

96328563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105624432-T-A

96328563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105624432-T-C

http://identifiers.org/hco/14/GRCh38#96328617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105624476-C-A

96328617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105624476-C-G

96328643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105624500-C-T

96328666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 105624519-T-A

96328666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 105624519-T-C

96328692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105624545-A-G

96328759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense variant
orthologous variants: 105624612-G-A

96328759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense variant
orthologous variants: 105624612-G-T

http://identifiers.org/hco/14/GRCh38#96328817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105624716-C-A

96328957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105624822-G-A

96328967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105624832-A-G

http://identifiers.org/hco/14/GRCh38#96328971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105624834-A-C

96328978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105624841-T-C

96329381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105624999-T-A

96329381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105624999-T-C

96329391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105625006-T-C

http://identifiers.org/hco/14/GRCh38#96329421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105625037-C-A

96329421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105625037-C-T

96329468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105625081-A-G

96329498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense variant
orthologous variants: 105625111-G-A

96329634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 105625247-T-A

96329634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 105625247-T-C

http://identifiers.org/hco/14/GRCh38#96329690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105625377-C-A

http://identifiers.org/hco/14/GRCh38#96329772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105625449-C-A

96329796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105625463-T-C

96330999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105626954-A-G

96330999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105626954-A-T

96331038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105626993-A-T

96331055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105627009-C-T

96331067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105627021-T-C

96331168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105627101-G-A

96331226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105627165-T-C

96331414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105627297-T-A

96331606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105627489-T-C

96331606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense variant
orthologous variants: 105627489-T-G

96331741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105627568-T-A

96331741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105627568-T-C

96331741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105627568-T-G

96331749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105627576-T-G

96331892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105627730-T-G

96331929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105627767-T-G

96332432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105628998-C-T

96332516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105629081-T-C

96332516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105629081-T-G

96332630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105629195-A-G

http://identifiers.org/hco/14/GRCh38#96332677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105629242-C-A

http://identifiers.org/hco/14/GRCh38#96332692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105629257-C-A

96332692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105629257-C-G

96332692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105629257-C-T

96332696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105629260-C-T

http://identifiers.org/hco/14/GRCh38#96332699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105629263-A-C

96332951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105629470-T-C

96333013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105629534-G-T

96333531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105630045-A-G

http://identifiers.org/hco/14/GRCh38#96333570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105630072-A-C

96333575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105630077-G-T

96333595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105630095-T-G

http://identifiers.org/hco/14/GRCh38#96333979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105630473-C-A

96334037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105630528-T-A

96334309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105630820-T-C

96334337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105630840-T-C

96334445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105630943-C-T

http://identifiers.org/hco/14/GRCh38#96334555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105631052-C-A

96334611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105631105-G-A

96334611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105631105-G-T

96334617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105631111-T-A

96334617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105631111-T-C

96334626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105631120-G-T

96334630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105631124-C-T

96334739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105631222-T-C

http://identifiers.org/hco/14/GRCh38#96334853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105631302-A-C

96335967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105631930-T-C

96336146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105632072-G-A

96336173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105632085-G-A

96336173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105632085-G-T

96336806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105632629-A-T

96341433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105632784-C-T

96341434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105632785-A-G

96341439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105632790-T-C

96341443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105632794-T-A

http://identifiers.org/hco/14/GRCh38#96341444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105632795-C-A

96341444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105632795-C-T

http://identifiers.org/hco/14/GRCh38#96341452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105632802-C-A

96341452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105632802-C-T

96341477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105632818-T-C

96341486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105632827-T-C

96341561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105632895-A-G

96341582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105632916-T-C

96341582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense variant
orthologous variants: 105632916-T-G

96341615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense variant
orthologous variants: 105632949-T-C

96341621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105632955-T-C

96341728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105633067-T-C

96341744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105633083-A-G

96341744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105633083-A-T

96344312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105636651-A-G

96344814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105637132-T-C

96344814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105637132-T-G

96344948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105637298-G-A

http://identifiers.org/hco/14/GRCh38#96345016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105637352-C-A

96345016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105637352-C-T

96345029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105637372-T-C

96345403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105637902-T-A

96345403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105637902-T-C

http://identifiers.org/hco/14/GRCh38#96345502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105637977-C-A

96345502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105637977-C-G

96345508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105637983-G-A

96345508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105637983-G-T

http://identifiers.org/hco/14/GRCh38#96345511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105637986-A-C

96345511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105637986-A-G

96345511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105637986-A-T

http://identifiers.org/hco/14/GRCh38#96345524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105637996-A-C

96345524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105637996-A-G

96345546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105638018-G-A

96347032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105640988-C-T

96347294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105641225-A-G

96347350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105641283-A-G

96347365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105641298-T-C

96347370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105641304-A-G

96347371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105641305-T-C

96347436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105641374-G-C

http://identifiers.org/hco/14/GRCh38#96347438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105641376-C-A

96357878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105645072-C-G

http://identifiers.org/hco/14/GRCh38#96358005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105645190-A-C

96358060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105645245-T-G

96358110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105645279-A-G

96358125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105645301-T-C

96358773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105645763-A-T

96358775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105645765-T-C

96358791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105645781-G-A

96358820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105645814-G-A

96358842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105645840-T-C

96359628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105646555-T-C

96359628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105646555-T-G

96360150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105646980-C-T

96360256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105647076-T-C

96360261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105647081-C-T

96360510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105647401-A-T

96360630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105647537-G-A

96361879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, undefined
orthologous variants: 105650106-T-A

96361901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105650123-T-C

96362375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron_variant, undefined
orthologous variants: 105650512-C-T

96362389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105650526-A-G

96362458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105650589-C-T

96362521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105650652-C-T

96362647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105650778-T-C

96362701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105650815-G-T

96362732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105650846-G-A

96362732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105650846-G-T

http://identifiers.org/hco/14/GRCh38#96362734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#105650848-C-A

96362734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105650848-C-T

96362751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: intron variant
orthologous variants: 105650865-A-G

96362862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: missense variant
orthologous variants: 105650975-G-C

96362863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: synonymous variant
orthologous variants: 105650976-G-A

96363014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5 prime UTR variant
orthologous variants: 105651145-T-A

96363014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5 prime UTR variant
orthologous variants: 105651145-T-C

96363072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5 prime UTR variant
orthologous variants: 105651222-G-A

96363072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5 prime UTR variant
orthologous variants: 105651222-G-T

http://identifiers.org/hco/14/GRCh38#96363144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#105651293-C-A

96363144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 105651293-C-G

96363144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 105651293-C-T

96363177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5 prime UTR variant
orthologous variants: 105651326-G-A

96363177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5 prime UTR variant
orthologous variants: 105651326-G-C

96363187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5 prime UTR variant
orthologous variants: 105651336-C-T

96363202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5 prime UTR variant
orthologous variants: 105651350-G-A

96363202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5 prime UTR variant
orthologous variants: 105651350-G-T

96363231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5 prime UTR variant
orthologous variants: 105651376-T-A

96363231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5 prime UTR variant
orthologous variants: 105651376-T-C

96363231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5 prime UTR variant
orthologous variants: 105651376-T-G

96363291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 105651430-T-A

96363291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 105651430-T-C

96363291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 105651430-T-G

96363313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20187
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 105651452-T-G