4726696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126787602-A-T

4726747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126787551-C-G

4726747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126787551-C-T

4726754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126787544-G-A

4726754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126787544-G-T

4726768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126787530-A-G

4726817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126787481-C-T

4726818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: synonymous variant
orthologous variants: 126787480-G-A

http://identifiers.org/hco/12/GRCh38#4739035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126782970-C-A

4739035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126782970-C-T

4739051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126782947-A-G

4739051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126782947-A-T

4739180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126782855-A-G

4739262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126782773-T-A

4739262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: synonymous variant
orthologous variants: 126782773-T-C

4739284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126782752-C-G

4739284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: stop gained
orthologous variants: 126782752-C-T

4739305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126782731-T-A

4739305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: synonymous variant
orthologous variants: 126782731-T-C

4739305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126782731-T-G

4739327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 126782710-A-G

4739331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: splice donor variant
orthologous variants: 126782706-T-A

4739331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: splice donor variant
orthologous variants: 126782706-T-C

http://identifiers.org/hco/12/GRCh38#4739344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126782693-C-A

4739372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126782664-A-G

4739392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126782660-A-G

4739401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126782651-T-C

http://identifiers.org/hco/12/GRCh38#4739433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126782619-A-C

http://identifiers.org/hco/12/GRCh38#4739481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126782571-C-A

4739587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126782465-C-T

4739636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126782417-C-G

4741015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126782124-G-A

http://identifiers.org/hco/12/GRCh38#4741078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126782064-A-C

4741082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126782060-G-A

4741389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126781761-C-T

http://identifiers.org/hco/12/GRCh38#4741489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126781667-C-A

4743477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126780968-T-G

http://identifiers.org/hco/12/GRCh38#4743626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126780619-C-A

4743972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126780166-A-T

http://identifiers.org/hco/12/GRCh38#4744365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126778953-C-A

4744365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126778953-C-T

4744375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126778943-A-G

http://identifiers.org/hco/12/GRCh38#4744376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126778942-C-A

4744376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126778942-C-T

http://identifiers.org/hco/12/GRCh38#4744387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126778931-C-A

4744417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126778887-G-A

4744417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126778887-G-T

4744424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126778880-G-A

4744424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126778880-G-T

http://identifiers.org/hco/12/GRCh38#4744433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126778872-C-A

4744444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126778861-T-A

4744444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126778861-T-C

4744489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126778814-T-C

4744496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126778807-A-G

4744573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126778721-G-A

4744573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126778721-G-C

4744573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: stop gained
orthologous variants: 126778721-G-T

4744622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126778672-C-G

4744782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126778520-T-A

4744782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126778520-T-G

http://identifiers.org/hco/12/GRCh38#4744911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126778282-C-A

4744912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126778281-T-A

http://identifiers.org/hco/12/GRCh38#4745220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126778009-C-A

4745287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777945-G-A

4745287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777945-G-C

4745342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777902-G-T

4745343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777901-G-A

4745343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777901-G-T

4745375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777873-C-T

4745452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126777802-T-C

4745479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126777775-C-T

4745481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126777773-C-T

4745500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126777754-G-A

4745542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126777712-A-G

4745542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126777712-A-T

4745604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126777653-C-T

4745617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126777640-C-T

4745630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777627-A-T

4745655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777612-A-G

4745738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777550-G-A

4745738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777550-G-T

4745762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777520-G-A

4745762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777520-G-T

4745898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777375-C-T

4745932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777359-G-A

4745932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777359-G-C

4745932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777359-G-T

4745959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777333-G-A

4745959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126777333-G-T

http://identifiers.org/hco/12/GRCh38#4746099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126776805-C-A

4746099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126776805-C-G

4746099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126776805-C-T

4746100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126776804-G-A

4746100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126776804-G-T

http://identifiers.org/hco/12/GRCh38#4746129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126776763-C-A

4746129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126776763-C-T

http://identifiers.org/hco/12/GRCh38#4746152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#126776740-C-A

4746198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: synonymous variant
orthologous variants: 126776694-C-T

4746211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense variant
orthologous variants: 126776681-G-C

4746261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126776631-G-A

4746302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126776590-G-A

4746382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126776512-T-C

4756412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126776094-C-G

4756413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126776093-T-C

4756445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126776061-A-G

http://identifiers.org/hco/12/GRCh38#4756646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126775897-C-A

4758314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126771989-C-G

4758529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126771810-G-A

4759128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126771165-A-T

4759818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126770162-A-G

http://identifiers.org/hco/12/GRCh38#4759819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126770161-C-A

4759847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126770133-C-T

4759848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126770132-G-A

4759848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126770132-G-C

4759858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126770122-T-C

4763289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126769507-A-G

4763433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769372-T-A

4763433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769372-T-C

4763434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769371-G-A

4763461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769315-T-G

http://identifiers.org/hco/12/GRCh38#4763467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126769306-C-A

4763467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769306-C-T

4763482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769291-A-T

http://identifiers.org/hco/12/GRCh38#4763490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126769283-C-A

http://identifiers.org/hco/12/GRCh38#4763491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126769282-C-A

4763491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769282-C-T

4763502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769271-T-C

http://identifiers.org/hco/12/GRCh38#4763521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126769230-C-A

4763521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769230-C-T

4763535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769208-T-C

4763559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769184-A-G

4763560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769183-T-C

4763588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769157-C-G

4763593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769152-C-G

4763618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769127-T-A

4763643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769111-T-C

4763643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769111-T-G

4763806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769024-G-A

4763806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769024-G-T

4763821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126769015-A-G

4763882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126768999-G-C

4763882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126768999-G-T

http://identifiers.org/hco/12/GRCh38#4763949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126768942-C-A

4763949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 126768942-C-T

4763957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126768934-A-G

http://identifiers.org/hco/12/GRCh38#4763960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126768931-C-A

4763960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126768931-C-T

4764042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126768861-T-C

4764047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 126768856-G-A

4764047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 126768856-G-C

4764101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126768823-C-G

http://identifiers.org/hco/12/GRCh38#4764109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126768815-A-C

4764109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126768815-A-T

http://identifiers.org/hco/12/GRCh38#4764134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126768787-A-C

4764155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126768768-G-A

http://identifiers.org/hco/12/GRCh38#4764156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126768767-C-A

4764156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126768767-C-G

4764156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126768767-C-T

4764158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126768765-G-C

4764205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126768742-C-T

4764238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126768706-G-A

4764317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126768632-T-C

4764317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126768632-T-G

4770421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126763662-A-G

http://identifiers.org/hco/12/GRCh38#4770558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126763568-A-C

http://identifiers.org/hco/12/GRCh38#4770704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126763456-A-C

4770829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126763306-A-G

http://identifiers.org/hco/12/GRCh38#4771847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126761700-A-C

4771945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126761620-G-A

4772013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126761557-C-T

http://identifiers.org/hco/12/GRCh38#4772024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126761546-C-A

4772278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126761340-G-A

4772420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126761228-T-C

4772441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 126761210-C-G

4772461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126761195-A-G

4772547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126761114-T-C

http://identifiers.org/hco/12/GRCh38#4772559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126761102-C-A

4772559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126761102-C-T

http://identifiers.org/hco/12/GRCh38#4772664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126761001-C-A

4772664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126761001-C-T

http://identifiers.org/hco/12/GRCh38#4772693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126760972-C-A

4772693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126760972-C-T

4772699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126760967-T-A

4772699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126760967-T-C

4772712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126760954-G-A

4772712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126760954-G-T

http://identifiers.org/hco/12/GRCh38#4772716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126760943-A-C

4772801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126760856-G-T

4772802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126760855-G-A

4772802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126760855-G-T

4772816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126760841-T-C

4772921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126760738-A-G

4772922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126760737-C-T

4773036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126760650-T-G

4773216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126760472-G-A

4775896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126755314-A-G

4775975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126755240-A-G

4776004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126755211-G-A

4776376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126754942-G-A

4776381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126754937-C-T

4776594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126754690-C-T

http://identifiers.org/hco/12/GRCh38#4779282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126750946-C-A

4779282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126750946-C-T

4779292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126750936-G-T

4779455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126750812-T-C

4779633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126750644-A-G

4779754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126750539-C-T

4780017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126750252-C-T

4780559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126749772-G-T

4780651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126749671-G-T

4780715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126749605-C-T

4780867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126749468-T-C

4781286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126748982-C-T

4781324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126748952-G-A

4781405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126748881-C-G

4781405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126748881-C-T

4781707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126748562-C-T

4781782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126748225-C-T

4785679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126747237-A-G

4785786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126747135-A-T

4785787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126747134-C-T

http://identifiers.org/hco/12/GRCh38#4785803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126747120-C-A

4785803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126747120-C-T

4786244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126746682-A-G

4786320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126746614-C-T

4786423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126746513-G-A

http://identifiers.org/hco/12/GRCh38#4786431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126746505-A-C

4786431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126746505-A-G

4786487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126746449-G-A

4786506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126746430-G-T

4786569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126746368-T-C

4786735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126746234-G-T

4786780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126746185-A-G

4786856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126746135-C-T

4787155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126745876-A-G

4787236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126745586-T-C

4787642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126745188-A-G

4787860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126745022-C-T

4787889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126744989-G-A

4788105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126744767-C-G

4788105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126744767-C-T

4788177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126744699-G-A

4788342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126744499-C-T

4788489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126744372-G-A

4788545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126744316-G-T

4788562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126744299-T-G

4788564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126744297-C-T

4788675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126744155-G-T

4788767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126744085-C-G

4788767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126744085-C-T

4788926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126743945-G-A

4788959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126743923-G-T

4789334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126742036-A-G

4792935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126735706-C-T

4792971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126735676-G-A

4793163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126735580-A-T

4793696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126733603-C-T

4793717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126733587-C-G

4793753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126733549-T-A

4793817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126733479-T-A

4793862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126733432-C-G

4794032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126733298-G-C

4794152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126733180-T-C

4794346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126732997-A-G

4794479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126732850-C-G

4794519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126732813-G-A

4794614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126732711-G-A

4794624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126732701-G-A

4794640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126732685-G-C

http://identifiers.org/hco/12/GRCh38#4796017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126730667-C-A

4796324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126730398-C-T

4796373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126730354-C-T

http://identifiers.org/hco/12/GRCh38#4796422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126730303-A-C

4796422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126730303-A-G

4796527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126730255-T-C

4796625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126730156-C-T

http://identifiers.org/hco/12/GRCh38#4796628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126730153-A-C

4796790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126730027-C-T

4796859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126729960-G-A

4796909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126729922-G-A

4797166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126729729-G-C

4797184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126729711-A-G

4797226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126729675-C-G

4797272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126729629-G-T

4797411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126729468-C-T

4797413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126729466-A-G

4797683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126729179-G-T

4798363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126728561-T-C

http://identifiers.org/hco/12/GRCh38#4798578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126728374-C-A

http://identifiers.org/hco/12/GRCh38#4798587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126728362-A-C

4798587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126728362-A-T

4798607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126728339-T-C

4798768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126727714-T-C

4798788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126727694-A-G

4799205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126727380-T-C

4799331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126727257-T-C

4799555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126727001-G-A

4799587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126726971-G-T

4799618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126726944-C-T

4799678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126726886-C-G

4799679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126726885-C-T

4800192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126726584-C-T

4800841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126725992-A-G

4800947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126725919-T-C

http://identifiers.org/hco/12/GRCh38#4801000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126725888-C-A

4802235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126723884-G-T

4802355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126723774-A-G

4802875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126723556-G-C

4803622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron variant
orthologous variants: 126722816-C-T

4806596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126719650-A-G

4806745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126719514-T-C

4807196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126719114-G-A

4808005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126718874-G-T

4808259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126718692-T-C

4808259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126718692-T-G

4808516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126718481-T-C

4808584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126718384-G-T

http://identifiers.org/hco/12/GRCh38#4808684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126718291-C-A

4808684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126718291-C-T

4808704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126718271-A-G

4808756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126718231-C-T

4808757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126718230-T-A

4808869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126718108-C-T

4808943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126718031-A-G

4809089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126717854-G-T

4809121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126717815-G-A

4809121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126717815-G-T

4809237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126717697-T-A

4809237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126717697-T-C

4809237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126717697-T-G

4809414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126717478-G-A

4809414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126717478-G-T

http://identifiers.org/hco/12/GRCh38#4809424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126717468-A-C

4809424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126717468-A-G

4809424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126717468-A-T

http://identifiers.org/hco/12/GRCh38#4809435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126717457-C-A

http://identifiers.org/hco/12/GRCh38#4809637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126717253-A-C

4809637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126717253-A-G

4809637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126717253-A-T

4809765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 126717124-G-A

4809765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 126717124-G-C

4809765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 126717124-G-T

http://identifiers.org/hco/12/GRCh38#4809954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#126716972-C-A

4809954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 126716972-C-T

4809984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 126716943-T-A

4809984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 126716943-T-C

4810021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126716906-G-A

4810021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126716906-G-T

4810036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126716891-G-A

4810036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126716891-G-T

4810116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 126716811-G-A

4810116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 126716811-G-C

4810116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 126716811-G-T

4810573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126716354-A-G

4811581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126715346-C-T

http://identifiers.org/hco/12/GRCh38#4811760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126715162-A-C

4811760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126715162-A-T

http://identifiers.org/hco/12/GRCh38#4811993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126714934-C-A

4812083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126714846-T-G

4812262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126714694-G-A

4812262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126714694-G-C

4812262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126714694-G-T

4812312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126714643-C-T

4812467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126714480-G-A

4812467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126714480-G-T

http://identifiers.org/hco/12/GRCh38#4812654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126714290-C-A

4812654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126714290-C-T

http://identifiers.org/hco/12/GRCh38#4812710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126714232-C-A

4812710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126714232-C-T

4812784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126714159-T-C

4812838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126714107-A-G

4812847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126714098-T-C

4812903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126714049-G-A

4812903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126714049-G-T

4813265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126713705-G-A

4813265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126713705-G-T

4813291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126713678-T-C

http://identifiers.org/hco/12/GRCh38#4813434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126713511-C-A

4813434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126713511-C-T

http://identifiers.org/hco/12/GRCh38#4813444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126713501-C-A

4813444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126713501-C-T

http://identifiers.org/hco/12/GRCh38#4813447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126713498-C-A

4813447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126713498-C-T

http://identifiers.org/hco/12/GRCh38#4813589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126713354-C-A

4813790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126713185-C-T

http://identifiers.org/hco/12/GRCh38#4813926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126713038-C-A

4813926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126713038-C-T

4814104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712869-A-G

4814125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712848-C-T

4814277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712702-T-A

4814277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712702-T-C

4814299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712674-T-G

4814357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712613-C-T

4814368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712605-A-G

http://identifiers.org/hco/12/GRCh38#4814410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126712561-C-A

4814436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712539-C-G

4814489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712490-A-G

4814570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712413-G-T

4814571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712412-A-G

http://identifiers.org/hco/12/GRCh38#4814603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126712377-C-A

4814616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712364-G-A

4814629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712351-G-A

4814629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712351-G-T

4814637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712334-A-G

4814668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126712299-A-T

http://identifiers.org/hco/12/GRCh38#4814794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126712165-C-A

4814799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126712160-G-T

4814800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126712159-G-T

4814845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126712134-G-T

4814874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126712121-T-C

4814885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126712110-A-G

4814890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126712104-G-T

http://identifiers.org/hco/12/GRCh38#4814912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126712082-C-A

4814988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126712024-G-T

4815115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126711936-T-C

4815219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126711839-A-G

4815497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126711533-G-T

4815665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126711390-G-A

4815692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126711363-A-G

4815705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126711351-C-T

4815754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126711304-T-G

4815834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126711224-C-T

4816178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126710940-T-C

4816179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126710939-C-T

4816191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126710927-G-T

4816231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126710886-T-C

4816414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126710275-T-C

4816420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126710269-G-A

4816459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126710258-T-C

4816514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126710203-A-G

4816525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126710192-A-G

4816689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126710133-T-G

4816747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126710083-C-T

4816836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126710000-C-T

4816849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126709994-C-G

4816926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126709929-C-G

4816955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126709898-C-T

4817063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126709775-A-G

4817063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126709775-A-T

http://identifiers.org/hco/12/GRCh38#4817287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126709571-C-A

4817287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126709571-C-T

4817608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126709309-A-G

4817718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126709194-T-C

4817759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126709155-T-A

4817821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126709068-C-G

4818034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126708828-G-C

4818042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126708824-A-G

4818541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126707966-C-T

4818635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126707801-A-G

4819206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126707167-C-G

4819206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126707167-C-T

4819333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126707055-C-T

4819538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126706823-C-T

4819549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126706815-G-T

4819595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126706768-A-G

4819846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126706388-G-A

4820008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126706258-C-T

http://identifiers.org/hco/12/GRCh38#4820484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126705763-A-C

4820509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126705742-A-G

4820945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126705366-T-C

4820981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126705330-C-G

4821193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126705107-T-A

4821292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126705009-T-C

4822865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126703982-T-C

http://identifiers.org/hco/12/GRCh38#4822915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126703924-C-A

4822964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126703876-G-A

4823174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126703112-A-G

4823229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126703056-C-T

4823475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126702850-C-T

4823877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126702785-G-T

4823983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126702715-G-A

4824022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126702689-T-C

4824461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126702297-C-T

4824809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126702003-C-G

4825112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126701407-T-G

4825311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126701214-C-G

4825330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126701195-T-A

4825337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126701188-A-G

4825431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126701108-T-C

4825517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126701015-G-A

4825519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126701013-A-G

4825554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126700974-A-G

4826426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126700837-C-G

4826426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126700837-C-T

4826704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126700559-A-G

4826881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126700372-G-T

4827099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126700237-T-C

4827193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126700182-C-T

4827460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126699955-G-T

4827560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126699878-G-T

4827653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126699797-C-T

4828810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126698168-C-G

4828810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126698168-C-T

4828868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126698116-C-T

http://identifiers.org/hco/12/GRCh38#4828928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126698079-A-C

4829722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126696955-G-T

4829753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126696924-C-T

http://identifiers.org/hco/12/GRCh38#4830013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#126696585-C-A

4830013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 126696585-C-T

4830258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126696382-A-G

4830440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126696149-C-T

http://identifiers.org/hco/12/GRCh38#4830581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126696034-C-A

4830613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 126695996-T-G

4830794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126695828-G-A

4830794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126695828-G-T

4831490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126695194-A-G

http://identifiers.org/hco/12/GRCh38#4831561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126695123-A-C

4837815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126693324-T-A

4837815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126693324-T-C

4837864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126693282-C-T

4838332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126692735-G-A

http://identifiers.org/hco/12/GRCh38#4838389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126692689-A-C

http://identifiers.org/hco/12/GRCh38#4850688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126685717-A-C

4850924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126685479-T-G

4851012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126685388-G-T

4851025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126685377-T-C

4851052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126685350-G-A

4851052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126685350-G-T

http://identifiers.org/hco/12/GRCh38#4851055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126685347-C-A

4851055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 126685347-C-T

4851116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126685288-G-A

4851120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126685284-T-A

4851120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126685284-T-C

4851205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126685200-T-C

http://identifiers.org/hco/12/GRCh38#4851317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126685099-A-C

4851317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126685099-A-G

4851346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126685070-G-A

4851392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126685025-G-T

4851498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126684841-T-A

http://identifiers.org/hco/12/GRCh38#4851548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126684692-C-A

4851565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126684674-G-A

4851565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126684674-G-T

4851677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126684581-A-G

4851679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126684579-G-T

4851685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126684573-G-T

4851724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126684544-G-A

4851724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126684544-G-T

4851766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126684486-G-T

4851769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126684483-T-G

http://identifiers.org/hco/12/GRCh38#4851780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126684472-C-A

4851820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126684436-G-T

4851894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126684384-A-G

http://identifiers.org/hco/12/GRCh38#4851905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#126684373-A-C

4851919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126684360-A-G

4851925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4130
most severe consequence: non coding transcript exon variant
orthologous variants: 126684354-G-T