44096059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: non coding transcript exon variant
orthologous variants: 77072997-G-A

44096059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: non coding transcript exon variant
orthologous variants: 77072997-G-C

44096070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: non coding transcript exon variant
orthologous variants: 77072985-G-A

44096070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: non coding transcript exon variant
orthologous variants: 77072985-G-C

44096083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: non coding transcript exon variant
orthologous variants: 77072972-T-C

44096093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: non coding transcript exon variant
orthologous variants: 77072962-A-G

44096170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: non coding transcript exon variant
orthologous variants: 77072886-A-G

44096216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: non coding transcript exon variant
orthologous variants: 77072842-C-T

44096403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: non coding transcript exon variant
orthologous variants: 77072653-A-G

44096534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: non coding transcript exon variant
orthologous variants: 77072534-T-A

44096617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: non coding transcript exon variant
orthologous variants: 77072451-C-G

44096688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: non coding transcript exon variant
orthologous variants: 77072382-G-A

44096726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: non coding transcript exon variant
orthologous variants: 77072347-A-G

http://identifiers.org/hco/13/GRCh38#44096933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77072076-A-C

44097326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77071885-A-G

http://identifiers.org/hco/13/GRCh38#44097568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77071646-A-C

44097568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77071646-A-G

44097703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77067166-C-T

http://identifiers.org/hco/13/GRCh38#44097907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77066948-A-C

44097907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77066948-A-G

44097923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77066932-A-G

44098021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77066889-A-G

44098046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77066864-T-A

44098068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77066846-T-C

44098069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77066845-C-T

http://identifiers.org/hco/13/GRCh38#44098512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77066738-A-C

44098512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77066738-A-G

44098626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77066618-G-A

44098633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77066612-T-G

44098947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77066299-C-T

44098993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77066255-A-G

44099043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77066229-T-C

44099194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77066065-C-T

44099201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77066060-G-A

44099209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77066052-C-T

44099343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77065890-A-G

http://identifiers.org/hco/13/GRCh38#44100126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77064867-A-C

44100188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77064804-A-G

44100290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77064697-G-A

44100436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77064471-C-T

44100598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77064258-G-T

44100697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77064144-A-T

44100920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77064015-T-C

44100936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77063999-T-C

44101386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77063584-G-A

44101386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77063584-G-C

44101386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77063584-G-T

44101402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77063570-G-A

44101501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77063459-A-G

44103908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77060752-C-G

44103908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77060752-C-T

44104072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77060589-C-T

44104086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77060575-C-T

44104440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77060216-C-T

44104650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77060003-C-G

44104992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77059694-C-G

44105070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77059622-A-G

44105145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77059551-G-A

44105146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77059550-C-G

44105224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77059467-T-C

44105244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77059446-A-T

44105427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77059301-A-G

44105475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77059280-G-A

44105475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77059280-G-T

44105651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77059093-T-A

http://identifiers.org/hco/13/GRCh38#44105849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77058858-C-A

44105921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77058782-T-G

44105948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77058755-A-G

http://identifiers.org/hco/13/GRCh38#44106225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77057519-C-A

44106225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77057519-C-T

44106270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77057478-A-G

44106445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77057314-G-T

44106581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77057194-A-G

44106667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77057101-T-G

http://identifiers.org/hco/13/GRCh38#44106762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77056975-C-A

44106762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77056975-C-G

44106773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77056939-T-G

44106867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77056713-C-T

http://identifiers.org/hco/13/GRCh38#44107047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77056448-C-A

44107047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77056448-C-T

44107048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77056447-C-T

44107061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77056428-A-T

44107151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77056350-G-A

44107151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77056350-G-T

44107162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77056339-T-C

44107167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77056334-T-A

44107211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77056311-T-G

44107212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77056310-G-A

44107212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77056310-G-T

44107297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77056240-T-C

44107382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77056163-A-G

44107463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77056095-G-A

44107803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77055783-C-T

44108051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77055544-G-T

http://identifiers.org/hco/13/GRCh38#44108069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77055523-C-A

44108091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77055491-G-A

44108113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77055469-C-G

44108405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77055197-G-A

44108405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77055197-G-C

http://identifiers.org/hco/13/GRCh38#44109127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77054538-A-C

44109135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77054528-C-T

http://identifiers.org/hco/13/GRCh38#44109213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77054472-C-A

44109213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77054472-C-T

44109224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77054461-A-G

44109554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77054131-G-A

http://identifiers.org/hco/13/GRCh38#44109724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77053941-C-A

44109724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77053941-C-T

44109851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77053802-A-G

44109940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77053721-T-C

http://identifiers.org/hco/13/GRCh38#44109973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77053686-C-A

44110222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77053569-T-C

44110222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77053569-T-G

44110419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77053378-A-G

44110434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77053361-G-A

http://identifiers.org/hco/13/GRCh38#44110438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77053357-C-A

44110438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77053357-C-T

44110506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77053292-T-C

44110893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77053184-C-G

44110990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77053085-C-T

44111001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77053074-T-A

http://identifiers.org/hco/13/GRCh38#44111189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77052900-C-A

44111189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052900-C-T

44111219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052860-C-G

44111475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052587-T-C

http://identifiers.org/hco/13/GRCh38#44111477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77052585-C-A

44111477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052585-C-T

44111565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052493-A-G

44111669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052394-A-G

44111669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052394-A-T

44111686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052376-G-T

44112012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052008-G-A

44112012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77052008-G-T

http://identifiers.org/hco/13/GRCh38#44112088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77051931-A-C

44112398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77051623-T-A

44112398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77051623-T-C

44112573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77051468-C-T

44112841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77051204-T-C

44112927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77051112-G-A

44114998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77050172-T-C

44115244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77049939-G-A

44115429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77049756-C-T

44115706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77049461-T-C

44115801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77049321-T-C

44116043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77049063-T-G

44116080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77049024-G-C

44116095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77049009-C-G

44116181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77048901-G-T

44116194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77048888-A-G

44116568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77048367-A-G

44116644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77048290-G-A

44116681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77048249-G-A

44116710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77048164-G-A

44116712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77048162-G-C

http://identifiers.org/hco/13/GRCh38#44116749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77048125-A-C

44116895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77047998-T-C

http://identifiers.org/hco/13/GRCh38#44116929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77047967-C-A

44116929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77047967-C-T

44116987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77047918-T-G

http://identifiers.org/hco/13/GRCh38#44117252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77042390-A-C

44117258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77042384-T-A

http://identifiers.org/hco/13/GRCh38#44117759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77041889-A-C

44117759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041889-A-T

44117762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041886-G-A

44118161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041540-G-C

44118199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041511-G-A

44118256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041454-T-C

44118256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041454-T-G

44118288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041422-C-T

44118372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041358-A-G

44118385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041345-T-C

44118405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041326-C-T

44118559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041172-T-C

44118563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041168-G-C

44118745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77041041-G-A

44118985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77040799-G-A

44119036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77038994-G-C

44119106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77038931-T-C

44119164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77038900-A-T

44119284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77038778-G-A

44119349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77038714-T-A

44119364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77038699-G-C

44119412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77038663-G-A

44119508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77038537-T-C

44119976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77037733-A-G

44120076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77037635-A-T

44120443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77037279-A-G

44121269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77036483-C-T

http://identifiers.org/hco/13/GRCh38#44121412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77036347-C-A

44121412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77036347-C-G

44121438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77036321-C-T

44124638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77031092-C-T

44124682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77031027-A-G

44124717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77030992-G-A

44124717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77030992-G-T

44125353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77030409-A-T

44125919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77030284-C-T

44126100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77030129-T-A

44126196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77030044-T-C

44126274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77029966-C-T

44126296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77029941-A-G

44126511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77029711-A-G

44126563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77029665-C-T

44126733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77029523-A-G

http://identifiers.org/hco/13/GRCh38#44127085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77029168-C-A

44127532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77029016-C-T

http://identifiers.org/hco/13/GRCh38#44127893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77027816-C-A

44128004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77027715-G-A

44128202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77027537-T-C

44128392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77027365-T-C

http://identifiers.org/hco/13/GRCh38#44128526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77027230-C-A

44128633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77027126-C-T

44128874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77026883-G-A

44128983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77026752-C-T

44129426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77026418-G-T

44132790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77025296-C-G

44133066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77025071-G-A

44133130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77025012-A-G

44133694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77024232-G-T

44135105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77023314-T-C

44135259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77023162-G-T

44135295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77023130-A-G

44135351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77023084-G-A

44135752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77022756-G-T

44135776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77022732-T-A

44135794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77022715-A-G

44136220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77018973-A-G

44136429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77018768-T-C

44136460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77018737-T-C

44136598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77018613-G-A

44136709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77018490-G-T

44137035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77018186-A-G

44137128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77018107-A-G

44137300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77017944-A-G

44137486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77017778-G-A

44137689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77017583-A-G

44137770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77017117-T-C

44137800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77017087-C-T

44139152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77016393-C-G

44139553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77016011-G-T

44139656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77015914-G-T

44139844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77015678-T-C

44140801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77014842-C-T

44141018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77014634-G-T

44141202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77014462-A-G

44141430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 77014220-C-G

44142738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77013839-T-C

44142778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77013817-G-T

44142800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77013795-A-G

44143192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 77013355-G-A

44143520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 77013030-T-C

44143742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77012834-G-T

44143949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77012671-G-A

44144014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77012615-A-T

44145730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77011460-A-G

44145760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77011431-A-G

44146967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77011142-G-A

44146967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77011142-G-T

http://identifiers.org/hco/13/GRCh38#44146968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77011141-C-A

http://identifiers.org/hco/13/GRCh38#44146980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77011130-C-A

44146980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77011130-C-T

http://identifiers.org/hco/13/GRCh38#44147000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#77011118-A-C

44147170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77010960-C-T

44147213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77010917-C-T

44147269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77010874-A-G

44147293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77010850-T-C