130672967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30610961-T-C

130672967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30610961-T-G

http://identifiers.org/hco/11/GRCh38#130672979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30610949-A-C

130673015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30610922-G-T

130673031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30610906-G-T

130673145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30610851-C-T

130673149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30610847-A-T

130673165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30610835-G-C

http://identifiers.org/hco/11/GRCh38#130673173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30610827-C-A

130673174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30610826-C-T

130673175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30610825-A-G

130673349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30610723-G-A

130673458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30610613-C-T

130673508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30610569-C-G

130673777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30610387-C-T

130673778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30610386-A-G

130673954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30610226-C-T

http://identifiers.org/hco/11/GRCh38#130673983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30610197-A-C

130674306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30609941-G-T

130674396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30609833-C-T

130674450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30609780-T-A

130674497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30609735-C-T

130674548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30609686-C-T

130674585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30609666-G-A

130674585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30609666-G-C

130674781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30609560-A-G

130674823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30609510-T-C

130675038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30609313-C-T

130675088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30608570-G-A

130675088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30608570-G-C

130675092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30608566-A-G

130675092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30608566-A-T

http://identifiers.org/hco/11/GRCh38#130675142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30608528-A-C

130676170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30608272-C-T

130676265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30608214-A-T

130676282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30608197-T-C

130676415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30608078-C-T

130676938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30601361-T-C

130676949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30601356-C-T

130677080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30601238-C-G

130677112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30601206-C-G

130677125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30601193-C-T

130677127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30601191-T-C

http://identifiers.org/hco/11/GRCh38#130677239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30601089-C-A

130677263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30601075-C-T

130677277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30601061-T-C

130677359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30600966-A-G

130677359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30600966-A-T

130677413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30600912-A-G

130677481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30600848-G-A

130677824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30600526-A-G

130677845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30600505-A-G

130677905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30600464-T-C

http://identifiers.org/hco/11/GRCh38#130687891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30597269-C-A

130687891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30597269-C-G

130687891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30597269-C-T

130687918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30597252-G-A

130688250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596927-C-T

130688267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596910-G-A

130688312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596859-G-C

130689252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596561-C-G

130689374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596437-A-G

130689495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596311-T-A

130689517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596289-T-C

130689569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596236-G-T

130689663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596124-T-C

http://identifiers.org/hco/11/GRCh38#130689679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30596108-C-A

130689784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30596004-C-G

130690016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595364-C-T

130690224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595188-G-A

130690250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595162-T-C

130690273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30595141-C-T

http://identifiers.org/hco/11/GRCh38#130690496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30593761-C-A

130691931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30593162-T-C

130692069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30593034-C-T

130692137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30592990-T-C

130692261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30592417-A-G

http://identifiers.org/hco/11/GRCh38#130692313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30592378-A-C

130692330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30592358-G-A

130692387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30592305-T-C

130692439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30592255-A-G

130692488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30592206-A-T

130692661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30592170-A-G

130692747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30592082-C-T

130692759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30592065-A-T

130692844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30591988-A-G

130692898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30591935-G-T

130693409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30591722-C-G

130693594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30591542-A-G

130694779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30588120-C-T

130695032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30587873-C-T

130695574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30587669-T-C

http://identifiers.org/hco/11/GRCh38#130696171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30587570-C-A

130696171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30587570-C-T

130696441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30587210-A-G

130696441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30587210-A-T

130696560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30587073-G-T

130696695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30586973-A-G

130696708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30586966-C-T

130696828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30586864-G-A

130696953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30586751-T-G

130697116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30586596-T-A

130698059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30585685-G-A

http://identifiers.org/hco/11/GRCh38#130698410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30585347-C-A

130698410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30585347-C-T

130698679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30585102-C-T

130698684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30585097-G-T

130698733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30585050-T-G

130698798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30585012-T-C

130699025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30584797-G-A

130699176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30584677-A-G

130704107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30573973-C-T

http://identifiers.org/hco/11/GRCh38#130704327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30573770-C-A

130704371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30573728-G-T

130705199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30566252-T-C

130705281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30566170-G-T

http://identifiers.org/hco/11/GRCh38#130705589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30565836-A-C

130705792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565655-A-G

130705812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565634-C-G

130705881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565561-G-C

130705960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565480-G-A

130706199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565240-C-G

http://identifiers.org/hco/11/GRCh38#130706207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30565232-A-C

130706226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30565213-T-A

130706442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30564942-A-G

130706830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30564575-C-T

130706915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30564487-C-T

130706951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30564451-T-A

130706974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30564429-A-G

130706974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30564429-A-T

http://identifiers.org/hco/11/GRCh38#130707022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30564394-C-A

130707049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30564367-T-C

130707111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30564309-G-A

130707337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30563840-C-T

130707369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30563809-T-C

130707530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30563647-C-T

130707727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30563460-G-A

130709507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30561873-T-C

130709544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30561836-G-A

130709682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30561684-C-T

130709949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30561442-G-A

130709950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30561441-G-T

130710071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30561322-T-A

130710120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30561276-C-T

130710258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30561158-T-C

130710480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30560934-C-T

130710751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30560658-G-C

130710820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30560576-G-A

130710820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30560576-G-C

130710885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30560524-T-G

130711058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30560372-G-T

130711174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30560297-T-A

http://identifiers.org/hco/11/GRCh38#130711186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30560285-C-A

130711383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552965-C-T

130711397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552951-G-A

130711488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552861-T-C

130711614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552784-G-C

130711795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552615-C-T

130711958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552503-T-C

130711958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552503-T-G

130711983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552480-G-A

130712289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30552165-T-A

http://identifiers.org/hco/11/GRCh38#130712307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30552147-A-C

130712463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30551239-G-T

130712560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30551146-T-A

130712560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30551146-T-C

http://identifiers.org/hco/11/GRCh38#130712695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30550020-C-A

130712698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30550017-T-C

130712703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30550012-C-G

130712766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549950-A-G

130713772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549561-C-T

130713792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549543-C-G

130713913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549439-T-C

130714028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549341-A-G

http://identifiers.org/hco/11/GRCh38#130714032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30549337-C-A

130714040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549329-G-A

130714040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549329-G-T

130714053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549314-A-G

130714055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549312-A-G

http://identifiers.org/hco/11/GRCh38#130714104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30549262-C-A

130714104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30549262-C-T

130714151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30549122-G-A

130714151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30549122-G-T

130714606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30548756-G-C

http://identifiers.org/hco/11/GRCh38#130714612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30548750-C-A

http://identifiers.org/hco/11/GRCh38#130714706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30548659-C-A

130714706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30548659-C-G

130714727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30548629-T-A

130714768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30548589-G-T

130714814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30548537-T-C

http://identifiers.org/hco/11/GRCh38#130714927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30548436-C-A

130714956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30548411-G-A

http://identifiers.org/hco/11/GRCh38#130714963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30548404-C-A

130714963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30548404-C-T

http://identifiers.org/hco/11/GRCh38#130715111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30548254-A-C

130715138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30548227-G-A

130715138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30548227-G-T

130715162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30548203-T-A

130715162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30548203-T-C

130715229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30548136-A-G

130715322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30548049-G-A

130715322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30548049-G-T

130715331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30548040-A-G

130715376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547995-T-A

130715401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547970-G-T

130715471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547899-G-T

130715525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547851-G-T

130715547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547830-A-G

130715573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547805-G-A

130715697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547679-C-T

130715701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547675-G-A

130715701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547675-G-T

130715877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547511-T-C

130715931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547456-G-T

http://identifiers.org/hco/11/GRCh38#130715954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30547415-C-A

130716034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547336-T-G

130716095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547277-G-C

130716191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547210-G-A

130716226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547174-T-G

130716335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547096-C-T

130716347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30547084-T-A

http://identifiers.org/hco/11/GRCh38#130716418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30547027-A-C

130716518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546938-A-G

http://identifiers.org/hco/11/GRCh38#130716663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30546796-C-A

130716751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546716-T-A

130716751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546716-T-C

130716789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546678-T-C

130716833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546633-T-C

http://identifiers.org/hco/11/GRCh38#130716930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30546558-A-C

130716952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546536-T-C

130716968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546528-T-C

http://identifiers.org/hco/11/GRCh38#130716976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30546520-C-A

130716976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546520-C-T

http://identifiers.org/hco/11/GRCh38#130716984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30546512-C-A

130716984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546512-C-T

130716995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546501-G-A

130716995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546501-G-T

http://identifiers.org/hco/11/GRCh38#130717045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30546464-C-A

130717078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546447-G-A

130717078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546447-G-T

130717079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546446-T-C

http://identifiers.org/hco/11/GRCh38#130717133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30546438-C-A

130717140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546431-A-G

http://identifiers.org/hco/11/GRCh38#130717146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30546425-C-A

130717146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546425-C-T

130717149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: 30546422-A-G

http://identifiers.org/hco/11/GRCh38#130717191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26805
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#30546380-C-A