2936923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34795392-T-C

http://identifiers.org/hco/4/GRCh38#2936931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34795403-C-A

2936931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34795403-C-T

http://identifiers.org/hco/4/GRCh38#2936946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34795413-C-A

2936950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34795418-T-C

2936976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34795444-G-A

2936976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34795444-G-T

http://identifiers.org/hco/4/GRCh38#2937014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34795461-C-A

http://identifiers.org/hco/4/GRCh38#2937015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34795462-C-A

2937116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34795515-C-G

2937121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34795520-T-C

2937121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34795520-T-G

http://identifiers.org/hco/4/GRCh38#2937126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34795525-C-A

2937126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34795525-C-G

2937136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34795532-T-C

2938948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796017-C-T

2938968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796036-A-G

2939034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796074-T-C

2939037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796077-G-A

2939037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796077-G-T

2939106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796129-G-A

2939106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796129-G-T

2939116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796144-C-G

2939116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796144-C-T

2939119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796147-T-C

2939120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796148-G-A

http://identifiers.org/hco/4/GRCh38#2939461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34796473-C-A

2939461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796473-C-T

2939512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796514-G-A

2939592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34796594-C-T

2939594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34796596-G-A

2939594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34796596-G-C

2939594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34796596-G-T

2939680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796692-T-C

2939720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796726-G-A

2939720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796726-G-T

2939743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796750-G-A

2939743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796750-G-C

2939743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796750-G-T

2939745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796752-G-A

2939794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796789-T-A

2939794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796789-T-C

2939863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796868-G-T

2939922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796939-G-A

2939933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796948-T-C

2940002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34797006-C-T

2940067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34797042-G-A

2940167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34797115-A-G

2940168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34797116-A-G

2940197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34797132-T-C

2940202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34797137-A-G

2940207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34797142-G-A

2940207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34797142-G-C

2940270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34797182-G-A

2940270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34797182-G-T

http://identifiers.org/hco/4/GRCh38#2940383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34797280-C-A

2940383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797280-C-T

2940518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797390-G-A

2940539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797402-G-A

2940539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797402-G-T

2940549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797412-C-T

2940649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797482-G-T

2940692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797507-G-A

2940692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797507-G-T

http://identifiers.org/hco/4/GRCh38#2940831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34797597-C-A

2940831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797597-C-T

2940836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797602-A-G

http://identifiers.org/hco/4/GRCh38#2940867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34797633-C-A

2940867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797633-C-G

2940867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797633-C-T

2940897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797662-A-G

2940916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797705-G-A

2940916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797705-G-T

http://identifiers.org/hco/4/GRCh38#2940988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34797775-C-A

2940988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797775-C-T

http://identifiers.org/hco/4/GRCh38#2940992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34797779-C-A

2940992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797779-C-T

2941012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797802-G-A

2941091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797870-A-G

2941104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797883-G-A

2941104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797883-G-C

2941104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34797883-G-T

2941472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34798108-G-A

2941472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34798108-G-T

2941501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34798137-G-T

http://identifiers.org/hco/4/GRCh38#2941536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34798170-C-A

2941536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34798170-C-T

2941542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34798175-T-C

2941601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798233-C-G

2941606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798238-G-A

2941606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798238-G-C

2941623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798255-T-G

2941647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798279-T-C

2941647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798279-T-G

2941671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798303-A-T

2941675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798307-G-A

2941687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798319-G-A

2941739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34798371-C-G

http://identifiers.org/hco/4/GRCh38#2941819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34798441-C-A

2941862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34798482-G-A

2941862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34798482-G-T

http://identifiers.org/hco/4/GRCh38#2941890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34798502-C-A

2941890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34798502-C-G

2941890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34798502-C-T

2941941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34798553-G-A

2941941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34798553-G-C

2941941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34798553-G-T

2942184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34798659-T-G

http://identifiers.org/hco/4/GRCh38#2942212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#34798687-C-A

2942212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798687-C-T

2942255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798730-C-G

2942274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798749-C-G

http://identifiers.org/hco/4/GRCh38#2942308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#34798783-C-A

2942308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798783-C-G

2942308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798783-C-T

http://identifiers.org/hco/4/GRCh38#2942415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34798886-C-A

2942415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34798886-C-T

2942425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34798887-C-T

http://identifiers.org/hco/4/GRCh38#2943925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34801121-C-A

2943925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34801121-C-T

2943926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34801122-A-T

2944030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34801226-A-G

2944046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34801247-G-A

2944046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34801247-G-C

2944046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34801247-G-T

http://identifiers.org/hco/4/GRCh38#2944070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34801267-C-A

2944070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34801267-C-G

2944086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34801283-G-C

http://identifiers.org/hco/4/GRCh38#2944134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#34801331-A-C

2944264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34801463-G-A

2944264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34801463-G-T

2944575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34801671-T-G

2945096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34802022-G-A

2945096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34802022-G-T

2945246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34802175-A-G

2945700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34803754-G-A

2945849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34803875-C-T

2946379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804469-G-A

http://identifiers.org/hco/4/GRCh38#2946433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#34804527-C-A

2946433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34804527-C-T

http://identifiers.org/hco/4/GRCh38#2946469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#34804563-A-C

2946469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34804563-A-G

2946498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34804592-T-C

2946498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34804592-T-G

2946514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34804608-T-A

2946514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34804608-T-C

2946552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34804646-T-A

2946552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34804646-T-G

2946574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804662-A-G

2946574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804662-A-T

2946659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804738-T-C

http://identifiers.org/hco/4/GRCh38#2946684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34804873-C-A

http://identifiers.org/hco/4/GRCh38#2946837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34805013-C-A

http://identifiers.org/hco/4/GRCh38#2946866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34805038-A-C

http://identifiers.org/hco/4/GRCh38#2946932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34805103-A-C

2946932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34805103-A-T

http://identifiers.org/hco/4/GRCh38#2946954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34805124-A-C

2946954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34805124-A-G

2946965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34805135-T-C

http://identifiers.org/hco/4/GRCh38#2946980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34805155-C-A

2946980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34805155-C-T

2946986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34805161-T-C

2946986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34805161-T-G

2947214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34805374-C-T

2947346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34805548-T-C

http://identifiers.org/hco/4/GRCh38#2947456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34805668-A-C

2947456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34805668-A-G

2947527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 34805737-C-G

2947555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34805765-T-C

2947631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34805841-G-T

2947641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34805849-T-C

2947642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34805850-C-T

2947684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34805891-T-G

2947774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34805970-C-G

2947800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34805992-G-A

2948004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34806441-C-G

http://identifiers.org/hco/4/GRCh38#2948167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34806582-C-A

http://identifiers.org/hco/4/GRCh38#2948182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34806588-C-A

2948182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34806588-C-T

2948196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34806599-G-A

2948196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34806599-G-T

2948214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34806617-C-G

2948214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34806617-C-T

2948232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34806637-G-A

2948235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34806640-A-G

http://identifiers.org/hco/4/GRCh38#2948238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34806643-C-A

2948238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34806643-C-T

2948246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34806651-C-G

2949545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34807300-T-C

2949792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34807525-A-G

2949792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34807525-A-T

2949794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34807527-G-A

2949794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34807527-G-T

2949796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34807529-G-A

2949796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34807529-G-T

2949805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34807538-G-T

2949806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34807539-G-A

2949806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34807539-G-T

http://identifiers.org/hco/4/GRCh38#2949867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34807578-C-A

2950040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34807776-G-A

2950040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34807776-G-C

2950251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34808000-G-A

2950251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34808000-G-T

2950435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34808460-G-A

2950435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34808460-G-T

2950436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34808461-G-A

2950436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34808461-G-T

http://identifiers.org/hco/4/GRCh38#2950449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34808474-C-A

2950449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34808474-C-T

http://identifiers.org/hco/4/GRCh38#2950465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34808490-C-A

2950465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34808490-C-T

2950491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34808515-T-C

http://identifiers.org/hco/4/GRCh38#2950581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34808609-C-A

2950595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34808623-G-A

2950595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34808623-G-T

2951001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34809005-G-A

2951001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34809005-G-T

2951130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34809110-C-T

2951138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34809118-A-G

2951162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34809142-A-G

2951181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34809161-A-G

2952233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34809550-G-A

2952233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34809550-G-T

2952265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34809629-G-A

2952265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34809629-G-T

http://identifiers.org/hco/4/GRCh38#2952271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34809636-C-A

2952271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34809636-C-G

2952281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34809646-C-T

2952427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34809787-T-A

2952489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34809821-T-A

2952491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34809823-A-G

http://identifiers.org/hco/4/GRCh38#2952525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34809860-C-A

2952525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34809860-C-T

2952815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34810296-C-T

2952928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34810460-G-A

2953350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34810861-C-T

2953366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34810874-G-A

2953366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34810874-G-T

2953494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811156-C-G

2953494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811156-C-T

2953497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811159-T-G

2953501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811203-T-C

2953505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811221-T-C

2953671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811390-C-G

2953703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811421-A-G

http://identifiers.org/hco/4/GRCh38#2953752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34811467-C-A

2953758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811473-G-A

2953758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811473-G-C

2953758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811473-G-T

2953763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811478-A-G

2953819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811514-C-T

http://identifiers.org/hco/4/GRCh38#2953871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34811561-C-A

http://identifiers.org/hco/4/GRCh38#2954330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34811705-C-A

2954496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34811852-G-A

2956320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813826-G-A

2956468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813931-C-T

2956484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813948-A-G

2956490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813954-T-A

2956540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814003-G-A

2956540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814003-G-C

2956540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814003-G-T

2956544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814007-T-A

2956544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814007-T-C

2956636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814064-G-A

2956636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814064-G-T

2956788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34814203-G-A

2956827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814246-A-T

http://identifiers.org/hco/4/GRCh38#2956916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34814316-C-A

2957029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814486-T-A

2957330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814888-G-A

2957355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814936-T-C

2957376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814979-G-A

2957589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34815202-C-G

2957687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34815300-G-C

2957693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34815306-A-G

2957779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20205
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34815397-T-G