185670933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82720635-A-G

185671122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82720823-A-G

185671405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82721046-G-A

185671405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82721046-G-T

185671413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82721054-C-T

185671444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82721074-A-G

185671471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82721101-G-T

185671538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82721134-A-G

185671556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82721152-T-G

http://identifiers.org/hco/2/GRCh38#185671989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82721576-C-A

185672017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82721604-G-C

185672182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82721771-T-C

185672370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82721956-A-G

185672499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82722052-T-C

185672514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82722067-A-T

185672621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82722101-G-A

185672654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82722129-T-G

185672867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82722328-T-C

185673132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82722565-G-C

185673685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82723859-T-C

185673788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82723971-A-G

185673788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82723971-A-T

http://identifiers.org/hco/2/GRCh38#185673839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82723995-A-C

185673894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82724053-G-A

185674051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82724193-G-T

185674253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82724390-T-C

185674865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82724966-T-C

185675043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82725051-G-C

185675095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82725065-G-T

http://identifiers.org/hco/2/GRCh38#185675663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82725572-A-C

185675663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82725572-A-G

185693414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82727967-T-C

185693474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82728028-G-A

185693530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82728079-A-G

185693768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82728355-C-G

185693782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82728391-A-G

185693919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82728594-G-C

185693919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82728594-G-T

185694659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82729481-G-A

185694763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82729592-A-G

185694863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82729686-T-C

185695144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82730277-A-G

185695267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82730402-C-T

185695325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82730451-T-A

185695325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82730451-T-C

185695490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82730628-A-G

185695619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82730759-A-G

http://identifiers.org/hco/2/GRCh38#185695990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82731098-A-C

185695990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82731098-A-G

185696103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82731198-T-C

185724186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82771257-G-A

185724213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82771319-G-T

http://identifiers.org/hco/2/GRCh38#185724247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82771353-C-A

185724247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82771353-C-T

http://identifiers.org/hco/2/GRCh38#185724324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82771426-C-A

185724324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82771426-C-T

185724360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82771461-G-A

185724370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82771471-G-A

185724370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82771471-G-T

185724459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82771561-T-A

185724459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82771561-T-G

185724690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82771826-G-A

185724690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82771826-G-T

185724751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82771876-G-A

185738168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773394-G-T

185738260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82773475-G-A

185738260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82773475-G-T

185738263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773478-T-A

185738263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773478-T-C

185738263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773478-T-G

185738266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773479-G-A

185738266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773479-G-C

185738266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773479-G-T

185738272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773485-A-G

185738323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773532-G-A

185738323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773532-G-C

185738323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773532-G-T

185738329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773538-G-A

185738329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773538-G-C

185738329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773538-G-T

http://identifiers.org/hco/2/GRCh38#185738346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82773548-A-C

185738346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773548-A-G

185738346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773548-A-T

185738358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773556-G-A

185738358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773556-G-T

185738393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82773589-T-C

185738723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82773914-G-A

http://identifiers.org/hco/2/GRCh38#185738725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82773916-A-C

185738725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82773916-A-G

http://identifiers.org/hco/2/GRCh38#185738777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82773949-C-A

185738777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82773949-C-T

185738989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82774140-G-A

185738989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82774140-G-C

185739051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82774165-G-A

185739051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82774165-G-T

185739142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82774225-G-A

185739143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82774226-T-A

185739163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82774247-G-A

185739163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82774247-G-T

185739244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82774315-T-C

185739274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82774345-G-A

185739274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82774345-G-T

185739288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82774359-T-C

http://identifiers.org/hco/2/GRCh38#185739303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82774376-C-A

185739303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82774376-C-T

185739480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82774548-G-A

185739480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82774548-G-C

185739480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82774548-G-T

185739487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82774568-T-A

185739487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82774568-T-C

185739537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82774605-G-A

185739537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82774605-G-T

185739619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82774669-T-C

http://identifiers.org/hco/2/GRCh38#185739648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82774699-A-C

185739648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82774699-A-G

185739969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82775008-T-C

185740172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82775248-T-C

185740325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82775383-G-A

185740326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82775384-T-G

http://identifiers.org/hco/2/GRCh38#185740365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82775416-A-C

185740365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82775416-A-G

http://identifiers.org/hco/2/GRCh38#185740372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82775423-C-A

185740381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 82775427-C-T

http://identifiers.org/hco/2/GRCh38#185740387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82775433-C-A

185740387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82775433-C-G

http://identifiers.org/hco/2/GRCh38#185740392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82775438-C-A

185740441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82775471-T-C

185741494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82775509-G-C

http://identifiers.org/hco/2/GRCh38#185741575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82775574-C-A

185741731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82775723-G-A

185741762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82775883-A-G

185741767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82775888-C-T

http://identifiers.org/hco/2/GRCh38#185741842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82775955-C-A

185741937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82776039-C-T

185741976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82776069-A-G

185742015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82776107-A-G

185742064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82776155-C-T

185742470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82776587-T-C

185742524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82776636-A-T

185742924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82777006-A-T

185743072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82777130-T-C

185743117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82777182-G-A

185743117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82777182-G-T

185743147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82777214-T-C

185743147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 82777214-T-G

http://identifiers.org/hco/2/GRCh38#185743313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82777385-C-A

185743313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82777385-C-T

http://identifiers.org/hco/2/GRCh38#185743395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82777961-C-A

185743395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82777961-C-T

185743403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82777969-T-G

185743406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82777972-G-A

185743406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82777972-G-T

http://identifiers.org/hco/2/GRCh38#185743427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82777993-C-A

185743612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82778158-G-T

185744293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82778523-T-C

185744477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82778689-G-A

185744477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82778689-G-C

185744477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82778689-G-T

http://identifiers.org/hco/2/GRCh38#185744516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82778724-C-A

185744516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82778724-C-G

185744516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82778724-C-T

http://identifiers.org/hco/2/GRCh38#185744625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82778823-C-A

185744641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82778859-G-A

http://identifiers.org/hco/2/GRCh38#185744651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82778879-A-C

185744675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82778904-T-A

185744785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82779009-G-A

185744823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82779057-T-G

185744832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82779066-T-C

185744883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82779098-G-A

185744974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82779241-G-A

185744974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82779241-G-T

185744988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82779255-T-G

http://identifiers.org/hco/2/GRCh38#185745023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82779294-C-A

185745023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82779294-C-G

185745050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82779317-G-A

http://identifiers.org/hco/2/GRCh38#185745071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82779328-C-A

185745071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82779328-C-T

185745097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82779353-G-A

185745097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82779353-G-T

185745108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82779363-A-G

http://identifiers.org/hco/2/GRCh38#185745297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82779601-A-C

185745297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82779601-A-T

http://identifiers.org/hco/2/GRCh38#185745476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82779780-C-A

185745632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82779942-T-A

185745632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82779942-T-C

185745632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82779942-T-G

185745660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82780060-T-A

http://identifiers.org/hco/2/GRCh38#185745709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82780320-C-A

185745988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82780600-G-T

185746044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82780666-G-T

185746185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82780792-T-C

185746303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82780875-C-T

185746408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82780975-G-C

185746421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82780988-C-T

http://identifiers.org/hco/2/GRCh38#185746428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82780995-C-A

http://identifiers.org/hco/2/GRCh38#185746605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82781175-C-A

185746605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82781175-C-T

185746741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82781297-G-T

185746757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82781313-C-T

185746823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82781379-A-G

185746835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82781387-T-A

185746835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82781387-T-C

185746835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82781387-T-G

185747157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82781842-A-G

http://identifiers.org/hco/2/GRCh38#185747217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82781889-C-A

http://identifiers.org/hco/2/GRCh38#185747222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82781894-A-C

185747222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82781894-A-T

185747245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82781919-G-A

185747245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82781919-G-T

185747280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82781955-A-G

185747381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82782056-A-G

185747418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82782093-A-G

185747418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82782093-A-T

185747506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82782196-A-G

http://identifiers.org/hco/2/GRCh38#185747526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82782220-C-A

185747526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82782220-C-T

185747536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82782230-T-G

http://identifiers.org/hco/2/GRCh38#185747552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82782261-C-A

185747786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82782628-A-G

http://identifiers.org/hco/2/GRCh38#185748219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82783307-C-A

185752827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82784522-G-A

185752827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82784522-G-T

185752961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82784643-T-G

185753070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82784758-T-C

185753160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82784822-T-C

185753316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82784964-C-T

185753500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785074-T-C

http://identifiers.org/hco/2/GRCh38#185753615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82785174-C-A

185753615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785174-C-T

http://identifiers.org/hco/2/GRCh38#185753648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82785206-C-A

185753648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785206-C-T

185753653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785211-T-G

185753658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785215-G-A

185753658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785215-G-T

185753685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785242-G-A

185753685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785242-G-C

185753691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785248-A-G

185753794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785348-G-A

185753794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785348-G-C

185753799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785353-A-G

185753867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785413-G-A

185753940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785479-T-C

185754063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785590-G-T

185754364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785931-T-A

185754423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82785970-A-G

185754506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82786040-A-T

185754684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82786200-G-C

185754761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82786278-T-C

185754763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82786280-T-A

185755240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82787969-A-G

185755286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82788015-T-C

185755650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82788453-G-T

185755671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82788474-G-A

185755688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82788491-T-C

185755814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82788617-G-C

185755814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82788617-G-T

185755859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82788654-T-C

185755917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82788715-G-C

185755917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82788715-G-T

185756010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82788810-T-C

http://identifiers.org/hco/2/GRCh38#185756053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82788850-C-A

185756053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82788850-C-G

185756053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82788850-C-T

185756173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82788958-T-C

185756179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82788964-A-G

185756179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82788964-A-T

185756217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789000-T-A

185756217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789000-T-C

185756293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789076-T-A

185756293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789076-T-C

185756308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789088-G-A

185756308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789088-G-T

185756309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789089-A-G

185756311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789091-A-G

185756311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789091-A-T

185756316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789098-A-G

185756316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789098-A-T

185756327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789109-G-A

185756327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789109-G-T

185756383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789162-T-C

http://identifiers.org/hco/2/GRCh38#185756485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82789239-A-C

185756524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789279-G-C

185756622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789373-A-G

185756690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789437-T-C

185756691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789438-G-A

185756934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82789673-G-T

http://identifiers.org/hco/2/GRCh38#185760877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82791945-C-A

185760877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82791945-C-T

http://identifiers.org/hco/2/GRCh38#185760883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82791980-C-A

185760883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82791980-C-T

185760914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82792016-G-A

185760914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82792016-G-T

185760951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82792040-A-G

185760951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82792040-A-T

http://identifiers.org/hco/2/GRCh38#185760969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82792049-C-A

185760969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82792049-C-G

185760969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82792049-C-T

http://identifiers.org/hco/2/GRCh38#185761117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82792192-C-A

185761117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82792192-C-T

185761169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82792233-A-G

185761235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82792297-T-C

185761515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82792558-C-G

185761659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82792697-G-T

http://identifiers.org/hco/2/GRCh38#185761994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82793061-A-C

185761994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82793061-A-G

185761994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82793061-A-T

185762047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82793099-T-C

185762054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82793106-T-C

185762784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82793228-T-C

http://identifiers.org/hco/2/GRCh38#185763047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82793492-A-C

185763047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82793492-A-G

http://identifiers.org/hco/2/GRCh38#185763168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82793609-C-A

185763174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82793615-T-C

185763178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 82793619-T-C

185763183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 82793624-G-T

185763292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82793730-A-G

185763292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82793730-A-T

185763307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82793745-T-C

http://identifiers.org/hco/2/GRCh38#185763342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82793777-C-A

185763601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82794026-A-G

185763633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82794059-A-G

185763688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82794109-T-A

185763737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82794157-G-A

185763797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82794214-A-G

185763994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82794422-C-G

185764272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82795566-G-A

http://identifiers.org/hco/2/GRCh38#185764400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82795677-A-C

185764413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82795690-G-C

185764413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82795690-G-T

185764468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82795730-G-A

185764468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82795730-G-C

185764468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82795730-G-T

185764589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82795854-A-G

http://identifiers.org/hco/2/GRCh38#185764600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82795865-C-A

185764600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82795865-C-T

185764614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82795879-T-C

185782314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82797724-G-A

http://identifiers.org/hco/2/GRCh38#185782645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82798058-C-A

185782645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82798058-C-T

http://identifiers.org/hco/2/GRCh38#185782652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82798065-C-A

185782667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82798080-G-A

185782681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82798092-T-C

http://identifiers.org/hco/2/GRCh38#185782722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82798133-A-C

185782722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82798133-A-G

185782722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82798133-A-T

185782837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82798236-G-C

185782837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82798236-G-T

185782933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82798331-G-A

185783427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82798958-T-A

185783427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82798958-T-C

185783451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82798982-A-G

185783574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82799107-G-C

185784171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82800928-A-G

185784207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82800962-T-C

185784841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82801476-T-C

185784879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82801513-T-C

185784911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82801544-G-A

185785184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82801751-C-T

185785725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82802862-A-G

185785833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82802974-G-A

185785872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82803013-C-G

185785976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82803086-G-C

http://identifiers.org/hco/2/GRCh38#185786038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82803157-C-A

http://identifiers.org/hco/2/GRCh38#185786095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82803217-A-C

185786103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82803225-G-A

185786103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82803225-G-T

185786141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82803268-G-C

185786264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82803389-G-A

185786319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82803444-A-G

185786820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82803949-C-T

185787065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82804181-G-C

185787065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82804181-G-T

185787201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82804305-T-C

185788080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 82804675-G-T

185788508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82805050-A-T

185788510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 82805052-T-C

http://identifiers.org/hco/2/GRCh38#185788572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#82805117-C-A

185788679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82805219-G-A

185788912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 82805443-A-G

http://identifiers.org/hco/2/GRCh38#185788928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82805459-C-A

185788928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 82805459-C-T

185788971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82805502-G-C

185789227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82805758-A-G

185789392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82805923-C-G

185789392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82805923-C-T

185789520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82806054-A-G

185789734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82806262-A-G

http://identifiers.org/hco/2/GRCh38#185790083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82806611-C-A

185790083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82806611-C-T

185790145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82806673-T-A

185790145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82806673-T-C

185790160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82806688-A-G

185790686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82807211-T-C

http://identifiers.org/hco/2/GRCh38#185790743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82807265-C-A

185790743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82807265-C-G

185790743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82807265-C-T

185790788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82807310-T-C

185790899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82807421-C-T

185791084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82807621-C-G

185791084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82807621-C-T

185791167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82807704-T-C

185791219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82807756-T-C

185791317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82807863-G-A

185791567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82808101-G-T

185791670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82808204-A-G

185791670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82808204-A-T

185791867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82808398-A-T

185792135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82808666-A-G

185792229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82808760-T-A

185792229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82808760-T-C

185792229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82808760-T-G

http://identifiers.org/hco/2/GRCh38#185792362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82808889-C-A

185792362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82808889-C-G

185792726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82809257-G-A

185792726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82809257-G-T

185792727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82809258-T-C

185792727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82809258-T-G

185792971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82809499-C-G

185792971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82809499-C-T

185793271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82809799-G-T

http://identifiers.org/hco/2/GRCh38#185793304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82809832-C-A

185793304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82809832-C-G

185793443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82809971-G-A

185793452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82809980-C-T

185793460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82809988-G-C

185793460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82809988-G-T

185793637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82810162-C-G

185793709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82810228-T-C

http://identifiers.org/hco/2/GRCh38#185793912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82810434-A-C

185793912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82810434-A-G

185794176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82810695-G-T

185794202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82810721-G-T

185794211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82810730-A-G

185794214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82810733-T-C

185794322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82810841-A-G

185794368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82810887-T-C

185794390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82810909-C-T

185794421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82810940-T-A

185794421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82810940-T-C

185794552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82811071-T-A

185794552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82811071-T-C

185794559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82811078-T-A

185794559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82811078-T-C

http://identifiers.org/hco/2/GRCh38#185794662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82811181-A-C

http://identifiers.org/hco/2/GRCh38#185794672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82811191-C-A

185794709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82811228-A-G

185794869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82811388-T-G

http://identifiers.org/hco/2/GRCh38#185794878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82811397-C-A

185794878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82811397-C-T

http://identifiers.org/hco/2/GRCh38#185794879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82811398-A-C

185794880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82811399-T-C

185794963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82811482-C-T

185795041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82811560-G-T

185795053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82811572-G-C

185795101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82811683-C-T

185795191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82811773-T-C

185795266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82811848-C-T

185795792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82812398-C-T

185795938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82812544-C-T

http://identifiers.org/hco/2/GRCh38#185795993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82812599-A-C

185796051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82812657-A-G

185796181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82812787-G-A

185796181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82812787-G-T

185796226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82812832-C-T

185796452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82813055-C-T

http://identifiers.org/hco/2/GRCh38#185796509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82813112-C-A

185796509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82813112-C-T

185796652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82813255-G-A

185796698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82813301-T-C

185796739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82813342-G-A

185796808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82813411-G-A

185796838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82813441-G-A

185797018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82813618-G-T

185797144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82813741-T-G

185797321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82813918-A-G

http://identifiers.org/hco/2/GRCh38#185797608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#82814203-C-A

185797608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82814203-C-G

185799359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82814590-C-T

185799548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82814616-A-G

185799710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82814723-A-G

185799889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82814902-G-T

185799909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40978
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 82814922-T-A