138825071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445864-T-G

138825098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445891-G-A

138825098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445891-G-T

138825113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445906-T-C

138825113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445906-T-G

http://identifiers.org/hco/3/GRCh38#138825115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445908-C-A

138825115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445908-C-G

138825115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445908-C-T

138825117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445910-T-A

138825117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445910-T-C

138825117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445910-T-G

138825125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445918-G-A

138825125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445918-G-T

138825128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445921-T-C

138825128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445921-T-G

138825138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445931-G-A

138825138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445931-G-T

138825145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445938-A-G

138825149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445942-A-G

138825149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445942-A-T

http://identifiers.org/hco/3/GRCh38#138825150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445943-C-A

138825150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445943-C-T

http://identifiers.org/hco/3/GRCh38#138825161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445954-C-A

138825161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445954-C-T

138825163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445956-T-C

138825163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445956-T-G

138825167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445960-T-A

138825167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445960-T-C

138825185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445978-T-A

138825197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445990-G-C

138825197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445990-G-T

http://identifiers.org/hco/3/GRCh38#138825203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445996-C-A

138825203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40445996-C-T

http://identifiers.org/hco/3/GRCh38#138825209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446002-C-A

138825209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446002-C-T

138825221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446014-T-C

http://identifiers.org/hco/3/GRCh38#138825230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446023-C-A

138825230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446023-C-G

138825230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446023-C-T

138825234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446027-G-A

138825234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446027-G-T

138825239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446032-T-A

138825239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446032-T-C

http://identifiers.org/hco/3/GRCh38#138825242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446035-C-A

138825250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446043-T-A

138825250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446043-T-C

138825260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446053-G-C

138825266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446059-T-C

http://identifiers.org/hco/3/GRCh38#138825267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446060-C-A

138825267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446060-C-T

138825268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446061-A-G

138825270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446063-G-A

138825270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446063-G-T

138825284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446077-T-C

138825287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446080-G-C

138825287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446080-G-T

138825293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446086-T-C

138825309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446102-G-A

http://identifiers.org/hco/3/GRCh38#138825329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446122-C-A

138825329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446122-C-T

138825335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446128-T-C

138825336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446129-G-A

138825336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446129-G-T

138825337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446130-G-C

138825337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446130-G-T

138825346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446139-G-A

138825346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446139-G-C

138825346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446139-G-T

http://identifiers.org/hco/3/GRCh38#138825348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446141-C-A

http://identifiers.org/hco/3/GRCh38#138825372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446165-C-A

138825372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446165-C-T

138825384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446176-G-A

138825384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446176-G-T

138825387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446179-A-G

138825390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446182-A-G

138825417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446212-T-A

138825417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446212-T-C

http://identifiers.org/hco/3/GRCh38#138825426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446221-C-A

138825426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446221-C-T

http://identifiers.org/hco/3/GRCh38#138825432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446227-C-A

138825432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446227-C-T

138825444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446239-T-A

138825444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446239-T-C

138825445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446240-G-A

138825445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446240-G-T

http://identifiers.org/hco/3/GRCh38#138825453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446248-C-A

138825453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446248-C-T

138825454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446249-A-G

138825454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446249-A-T

138825471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446266-T-C

http://identifiers.org/hco/3/GRCh38#138825498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446293-C-A

138825498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446293-C-G

138825498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446293-C-T

138825520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446315-A-G

138825533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446328-A-G

138825556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446351-A-G

138825556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446351-A-T

http://identifiers.org/hco/3/GRCh38#138825564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446359-C-A

138825567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446362-G-A

138825567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446362-G-T

138825579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446374-G-A

138825579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446374-G-C

138825579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446374-G-T

138825589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446384-G-C

138825589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446384-G-T

http://identifiers.org/hco/3/GRCh38#138825595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446390-C-A

138825597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446392-T-A

138825597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446392-T-C

138825600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446395-A-G

138825608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446403-A-G

http://identifiers.org/hco/3/GRCh38#138825612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446407-C-A

138825612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446407-C-G

138825618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446413-A-G

138825623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446418-T-C

138825624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446419-G-A

138825624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446419-G-T

138825625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446420-C-G

138825625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446420-C-T

138825627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446422-A-G

138825627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446422-A-T

138825636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446431-T-A

138825636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446431-T-C

138825637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446432-C-G

138825642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446437-C-T

138825643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446438-T-A

138825643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446438-T-C

http://identifiers.org/hco/3/GRCh38#138825649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446444-C-A

138825651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446446-A-G

http://identifiers.org/hco/3/GRCh38#138825661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446456-C-A

138825661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446456-C-G

138825661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446456-C-T

http://identifiers.org/hco/3/GRCh38#138825664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446459-C-A

138825698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446493-A-G

138825698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446493-A-T

138825710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446505-C-T

http://identifiers.org/hco/3/GRCh38#138825730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446525-C-A

http://identifiers.org/hco/3/GRCh38#138825738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446533-C-A

138825738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446533-C-T

138825750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446545-T-A

138825751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446546-G-A

138825751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446546-G-T

http://identifiers.org/hco/3/GRCh38#138825763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446558-C-A

138825763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446558-C-T

http://identifiers.org/hco/3/GRCh38#138825792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446587-C-A

138825823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446620-G-A

138825823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446620-G-T

138825840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446637-G-A

138825840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446637-G-C

138825840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446637-G-T

138825842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446639-G-T

138825879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446676-A-G

http://identifiers.org/hco/3/GRCh38#138825888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446685-C-A

138825888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446685-C-T

138825889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446686-T-C

138825906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446703-A-G

138825934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446731-T-G

http://identifiers.org/hco/3/GRCh38#138826009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446806-C-A

138826009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446806-C-T

138826027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446824-T-C

138826027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446824-T-G

138826039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446836-T-C

138826078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446874-T-C

138826093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446889-G-A

138826093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446889-G-C

138826093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446889-G-T

138826124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446921-G-A

138826124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446921-G-T

138826133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446930-T-C

138826137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446934-G-A

138826137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446934-G-T

138826140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446937-G-A

138826140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446937-G-T

138826148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446945-T-C

138826152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446949-A-G

138826157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446954-T-C

138826171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446968-T-C

138826174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446971-A-G

138826181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446978-G-A

138826181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446978-G-C

138826190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446987-G-T

138826191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446988-G-A

138826191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446988-G-T

138826196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446993-T-A

138826196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446993-T-C

138826199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446996-T-A

138826199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446996-T-C

http://identifiers.org/hco/3/GRCh38#138826201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446998-C-A

138826201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446998-C-G

138826201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446998-C-T

138826202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40446999-T-C

http://identifiers.org/hco/3/GRCh38#138826203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447000-C-A

138826205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447002-G-T

138826211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447008-T-C

138826222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447019-G-A

138826222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447019-G-C

138826222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447019-G-T

http://identifiers.org/hco/3/GRCh38#138826233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447030-C-A

138826235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447034-G-C

138826235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447034-G-T

http://identifiers.org/hco/3/GRCh38#138826242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447041-C-A

138826242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447041-C-T

138826256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447055-A-T

138826273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447072-G-T

138826276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447075-G-A

138826276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447075-G-T

http://identifiers.org/hco/3/GRCh38#138826283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447082-C-A

138826283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447082-C-G

138826283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447082-C-T

138826286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447085-G-A

138826286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447085-G-T

http://identifiers.org/hco/3/GRCh38#138826298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447097-A-C

138826298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447097-A-G

138826327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37898
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 40447126-T-G