11649790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5 prime UTR variant
orthologous variants: 134012738-G-A

11649790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5 prime UTR variant
orthologous variants: 134012738-G-C

11649790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5 prime UTR variant
orthologous variants: 134012738-G-T

11649823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5 prime UTR variant
orthologous variants: 134012789-T-G

11649844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5 prime UTR variant
orthologous variants: 134012809-C-T

11649991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 134012931-G-A

11650369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134013298-G-A

11650369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134013298-G-C

11650420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134013562-A-G

http://identifiers.org/hco/12/GRCh38#11650523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134013658-C-A

11650523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134013658-C-G

11650523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134013658-C-T

http://identifiers.org/hco/12/GRCh38#11650540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134013675-C-A

11650540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134013675-C-T

11650563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134013698-G-T

11650870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134014033-G-C

11651123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134014300-A-G

11651622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134014746-T-G

11651692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134014807-G-A

11651758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134014877-A-G

11651814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134014935-C-G

11651846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134014967-A-G

11651917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134015064-T-C

11652271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134015532-G-A

11652764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134016101-T-C

11652789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134016126-T-C

11652833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134016168-T-C

11652842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134016177-C-G

11652842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134016177-C-T

11652944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134016218-G-A

11652944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134016218-G-T

http://identifiers.org/hco/12/GRCh38#11653055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134016298-C-A

11654016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134017107-G-C

11654654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134017510-G-C

11654890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134017705-C-G

11655061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134017845-G-A

11655180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134017939-T-G

11655283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018045-G-C

11655435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018192-G-T

11655519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018277-A-G

11655628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018391-A-G

11655787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018561-T-G

11655827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018583-T-C

11655865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018624-C-T

11655891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018649-G-A

11655897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018663-C-T

11656189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018922-C-G

11656196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134018929-A-G

11656445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134019145-C-G

11656488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134019184-T-C

11656781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134019459-T-G

http://identifiers.org/hco/12/GRCh38#11656820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134019488-A-C

11656820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134019488-A-T

11657395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134020426-C-T

11657619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134020670-G-A

11657995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021041-G-A

11657995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021041-G-C

11658827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021522-G-A

11658943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021618-A-G

11658986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021644-G-A

11659129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021784-G-A

11659129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021784-G-C

11659291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021945-G-A

11659307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134021961-T-A

http://identifiers.org/hco/12/GRCh38#11659587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134022572-A-C

11660699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134023246-C-T

11660815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134023322-C-T

11660827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134023334-T-C

11660828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134023335-A-T

11661671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134023969-C-T

11661833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134024111-A-G

11661991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134024241-A-G

11662027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134024278-G-T

11662197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134024869-G-A

11662239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134024914-G-T

11662374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134025044-A-G

11662619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134025269-T-C

11662903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134026131-G-A

11662945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134026156-C-G

11663107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134026304-T-A

11663148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134026347-T-C

11663255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134026451-T-C

http://identifiers.org/hco/12/GRCh38#11663329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134026525-A-C

11663329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134026525-A-G

11663408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134026604-A-G

11663490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134026690-A-G

11663508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134026708-T-A

11663515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134026715-T-C

11663873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134027079-A-T

11664036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134027253-A-G

11664086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134027304-A-G

11664159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134027369-G-A

11664159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134027369-G-C

11664159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134027369-G-T

11664160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134027370-T-C

11664403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134027615-G-C

11664467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134027691-T-C

11664516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134027735-T-C

11664620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134027804-G-A

11665286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134029068-A-T

11665289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134029071-A-G

11665474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134029264-A-G

11665887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134029860-G-C

11665926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134029895-G-T

11666041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134030001-G-C

11666041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134030001-G-T

11666192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134030110-G-A

11666400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134030318-A-G

11666471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134030386-C-T

11666525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134030436-T-G

11666775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134030682-G-A

11666775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134030682-G-C

11666846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134030751-T-C

11666912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134030816-G-A

11668575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134031652-G-A

11668575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134031652-G-T

11668741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134031792-C-T

11669575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134032479-C-T

11669611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134032515-T-C

11669712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134032604-C-T

11669792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134032684-T-C

11669839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134032693-T-C

http://identifiers.org/hco/12/GRCh38#11669959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134032786-C-A

11669985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134032807-T-G

11669986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134032808-C-T

11670075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134032858-G-A

11670092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134032874-A-G

11670202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134032985-G-T

11670238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134033051-G-A

11670288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134033097-C-T

11670293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134033102-G-A

11670334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134033160-G-A

11670357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134033187-G-A

11670374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134033204-A-T

11671700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035045-C-T

11671989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035472-T-A

11671989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035472-T-G

http://identifiers.org/hco/12/GRCh38#11671994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134035473-C-A

11671994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035473-C-T

11671997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035476-T-C

11672223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134035689-A-G

11672883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134036330-C-T

http://identifiers.org/hco/12/GRCh38#11672907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134036354-C-A

11673929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037746-A-G

11673961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037769-T-C

11674132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037936-T-C

11674150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134037954-A-G

11674259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134038061-C-G

11674286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134038088-A-G

11674323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134038125-G-C

http://identifiers.org/hco/12/GRCh38#11674694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134038432-C-A

11674881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134038570-G-A

http://identifiers.org/hco/12/GRCh38#11675055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134038721-A-C

11675055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134038721-A-G

11676033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134039607-C-T

11676317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134039898-T-C

11676460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134040106-G-A

http://identifiers.org/hco/12/GRCh38#11676713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134040404-A-C

11677250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134041210-G-C

11677282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134041258-C-T

11677427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134041404-C-T

11677455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134041430-C-T

11677462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134041437-G-T

11677731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134042217-C-T

11677941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134042409-G-T

11678050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134042468-A-G

11678083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134042484-A-G

11678139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134042536-A-G

11678249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134042638-A-G

11678636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134042983-G-C

11678636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134042983-G-T

11678667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134043033-C-T

http://identifiers.org/hco/12/GRCh38#11678675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134043041-A-C

11678675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134043041-A-G

11678700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134043071-A-G

11678839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134043192-A-G

11678861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134043214-A-G

11679181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134043557-A-G

11679250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134043641-C-T

11679379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134043699-G-A

11679402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134043711-G-A

http://identifiers.org/hco/12/GRCh38#11679750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134044007-C-A

11679750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134044007-C-G

11679764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134044026-T-G

11680008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134044619-C-T

11680068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134044672-T-A

http://identifiers.org/hco/12/GRCh38#11680203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134044790-C-A

11680261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134044832-G-T

11680525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134045590-T-C

11680559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134045604-G-A

11680596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134045641-G-A

11680596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134045641-G-C

http://identifiers.org/hco/12/GRCh38#11683576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134046977-C-A

11683881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134047284-A-T

11684209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134047568-G-A

11684268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134047622-C-T

11684285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134047645-A-G

11684497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134048660-A-G

11684535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134048696-A-G

11684571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134048732-G-A

11684571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134048732-G-C

11684706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134048862-C-G

11684706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134048862-C-T

11685000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134049116-G-A

11685120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134049197-C-T

11685275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134049279-T-G

11685358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134049399-T-A

11685630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134049636-A-G

11685771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134049777-T-C

11686025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134050016-A-G

11686437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134050312-C-T

11686460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134050334-C-T

11687879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134051125-A-G

11688428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134051615-G-A

11688428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134051615-G-T

11688624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134051809-C-T

11688665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134051836-G-C

11688773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134051946-G-A

11688977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134052140-C-T

11689081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134052245-C-T

11689203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134052344-C-T

http://identifiers.org/hco/12/GRCh38#11689776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134053322-A-C

http://identifiers.org/hco/12/GRCh38#11689779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134053325-C-A

11689795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134053341-G-T

11690080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134053617-C-T

11690118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134053655-A-T

11690288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134053789-A-G

11690290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134053791-G-A

11692449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134054867-A-G

11692471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134054889-C-T

11692728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134055140-G-A

11693290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134055771-C-T

11693397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134055882-C-T

http://identifiers.org/hco/12/GRCh38#11693824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134056277-C-A

11693858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134056311-G-T

11694175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134056636-C-T

11694730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134057325-C-T

11694734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134057329-A-G

11694842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134057432-C-G

11695106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134057706-A-G

http://identifiers.org/hco/12/GRCh38#11695276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134057892-A-C

11695341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134057974-A-G

11695365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134058000-A-G

11695381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134058021-C-T

11695459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134058073-C-G

11695578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134058181-A-G

11695641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134058246-T-C

11695677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134058295-G-T

11695684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134058302-T-C

11695709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134058327-G-C

11696012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134058594-A-T

11696029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134058611-A-T

11697084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134059626-A-G

11697140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134059662-A-T

11697259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134059789-C-T

11697349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134059876-G-A

11697370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134059897-G-A

http://identifiers.org/hco/12/GRCh38#11698551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134060760-C-A

11698725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134060906-G-A

11698725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134060906-G-C

11698725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134060906-G-T

http://identifiers.org/hco/12/GRCh38#11699045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134061216-C-A

11699253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134061573-G-A

11699277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134061591-A-G

11701086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134062524-T-G

11701113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134062563-A-T

11701136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134062586-T-C

11701153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134062603-G-T

11701218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134062668-A-G

11701223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134062673-C-T

11701437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134062866-T-C

11701437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134062866-T-G

11701491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134062936-A-G

http://identifiers.org/hco/12/GRCh38#11701567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134063183-C-A

11701567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134063183-C-T

11701791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134063387-G-A

11701807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134063403-C-T

11701888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134063499-G-A

11701944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134063555-G-A

11702026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134063636-C-T

http://identifiers.org/hco/12/GRCh38#11702457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134064030-A-C

11703302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134064861-A-G

11703368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134064932-G-A

11703406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134064963-A-G

11703513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065257-T-A

11703513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065257-T-C

11703545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065289-T-A

11703548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065292-G-C

11703625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065341-G-A

11703643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065359-T-A

11703643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065359-T-G

11703657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065373-T-C

11703761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065464-C-T

11703787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065490-A-G

11703871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065568-A-G

http://identifiers.org/hco/12/GRCh38#11704077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134065763-A-C

11704077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065763-A-G

11704212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134065882-C-G

11705373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134066256-G-A

11705377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134066260-G-A

11705561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134066529-G-T

11705698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134066687-G-A

11706192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134067121-A-G

11706761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134068252-C-T

http://identifiers.org/hco/12/GRCh38#11707122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134068611-A-C

11707306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134069504-G-T

11707385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134069594-G-A

11707476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134069687-T-C

11707714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134069945-G-A

11707714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134069945-G-T

11707781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134070014-A-G

11707781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134070014-A-T

11707928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134070710-T-C

http://identifiers.org/hco/12/GRCh38#11707978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134070749-C-A

11708131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134070917-C-T

11708145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134070931-C-T

11708184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134070990-G-A

11708228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071039-T-A

11708328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071068-C-T

http://identifiers.org/hco/12/GRCh38#11708534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134071273-C-A

11708534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071273-C-G

11708605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071342-G-A

11708816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071549-G-A

11709028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071730-T-G

11709104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071790-T-C

11709127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071813-T-G

11709157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071844-A-G

11709228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071880-C-T

http://identifiers.org/hco/12/GRCh38#11709312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134071948-C-A

11709312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071948-C-G

11709312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134071948-C-T

11709525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134072432-A-G

11709536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134072447-G-A

11709660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134072560-G-A

http://identifiers.org/hco/12/GRCh38#11709809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134072685-C-A

11709868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134072740-C-T

11709970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134072860-C-G

11710018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134072915-G-A

11710037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134072939-T-C

11710072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134072974-A-G

11710083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134072985-C-T

http://identifiers.org/hco/12/GRCh38#11710086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134072988-A-C

11710235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134073127-A-T

11710562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134073470-T-C

11710582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134073490-C-T

11710849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134073954-G-A

11710867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134073980-G-A

11710872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134073985-C-T

11711586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134074618-G-A

11711612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134074636-G-A

11711981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134074956-T-C

11712268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134075116-G-C

11712333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134075180-A-G

11712667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134075610-T-A

11712946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134075970-G-A

11712946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134075970-G-C

http://identifiers.org/hco/12/GRCh38#11713057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134076068-A-C

http://identifiers.org/hco/12/GRCh38#11713116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134076122-A-C

11713139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134076168-T-C

11713299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134076349-G-A

http://identifiers.org/hco/12/GRCh38#11713392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134076472-C-A

11713525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134076584-C-T

11713603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134076675-G-A

11713710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134076772-A-G

11713783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134076844-T-C

11714290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134077371-A-G

11714458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134077537-T-C

11714737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134077803-A-G

11714773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134077840-T-C

11714782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134077849-C-T

http://identifiers.org/hco/12/GRCh38#11714863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134077930-C-A

11714863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134077930-C-T

11715170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134078165-C-G

11715170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134078165-C-T

11715552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134078833-G-T

11715583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134078864-G-A

11715624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134078905-C-T

11715845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134079129-C-T

11715985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134079629-G-A

11716001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134079645-G-A

11716320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134079676-G-A

11716320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134079676-G-C

11716320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134079676-G-T

11716381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134079711-G-T

11716417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134079747-G-A

11716566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134079899-T-C

11716628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134079946-T-C

11716675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134079984-A-T

11716696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134080005-A-G

11716770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134080077-T-A

11716888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134080192-T-C

http://identifiers.org/hco/12/GRCh38#11717475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134080777-C-A

11717475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134080777-C-G

11717511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134080811-G-A

11717991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134081591-A-G

http://identifiers.org/hco/12/GRCh38#11718132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134081730-A-C

11718932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134082193-C-T

11718994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134082233-T-A

11718994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134082233-T-C

11719031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134082267-A-G

11719031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134082267-A-T

11719278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134082410-G-T

11719679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134082801-A-G

11719743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134082860-G-A

11719807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134082918-C-T

11719877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134082982-G-A

11719877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134082982-G-T

11720181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134083214-A-G

11720231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134083257-A-G

11720284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134083310-A-G

11720311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134083341-A-G

11721862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134083627-T-C

11722348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134084042-T-A

11722350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134084044-A-G

11722694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084361-C-T

11722758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084424-G-A

11722848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084508-G-A

11722883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084543-G-A

11722959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084606-C-G

11723139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084759-G-A

11723182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084802-A-G

11723227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134084830-G-A

11723511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134085077-C-T

http://identifiers.org/hco/12/GRCh38#11723771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134085338-A-C

11723788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134085354-C-T

11723823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134085393-G-C

11723907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134085575-G-C

11723973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134085634-G-A

11724066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134085703-C-T

11724161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134085790-G-T

11724296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134085911-G-C

11724754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134086299-G-C

11724754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134086299-G-T

11724769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134086314-C-G

11724859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134086565-A-G

11725013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134087072-T-A

11725194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134087192-A-T

11726229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134087734-G-A

11728712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134087776-C-T

11728864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134087890-C-G

11729025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134088479-T-C

11729054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134088508-C-G

11729135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134088588-T-C

11729140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134088593-A-G

11729567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134089039-G-C

11729567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134089039-G-T

11729940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134089874-C-T

11730001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134089936-A-G

11730009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134089958-G-A

http://identifiers.org/hco/12/GRCh38#11730696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134090579-C-A

11730696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134090579-C-T

11730978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134090839-C-T

11731011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134090870-T-A

11731058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134090919-C-G

11731182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134091035-G-A

11731209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134091062-T-C

11731257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134091104-C-G

11731568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134091381-G-A

11731568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134091381-G-T

11731731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134091528-C-T

11731920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134091719-T-C

11731970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134091762-C-T

11732085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134091843-G-A

11732506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134092465-C-T

11732549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134092506-G-A

11732607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134092562-G-A

11733004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134092900-A-G

11733460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134093294-C-G

11733460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134093294-C-T

11733581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134093409-T-C

11733581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134093409-T-G

11733587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134093415-C-G

11733771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134093708-A-G

11733782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134093719-C-T

11733822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134093759-G-A

11734073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134094018-A-G

11734192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134094135-A-G

11736588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134096710-T-C

11736599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134096721-C-G

11736646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134096759-A-G

11736760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134096855-T-C

11737136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134097221-A-G

11737487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134097551-T-C

11737763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134097840-A-T

11737985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134098039-C-T

http://identifiers.org/hco/12/GRCh38#11738642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134098476-C-A

11738706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134098531-T-G

11738852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134098694-C-T

11738894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134098736-G-A

11738894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134098736-G-T

11739178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134098902-C-T

http://identifiers.org/hco/12/GRCh38#11739327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134099018-A-C

11739327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099018-A-G

11739396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099113-A-G

11739430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099147-G-A

11739757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099723-A-T

11739939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134099853-C-T

11740102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134100009-G-A

11740147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134100060-G-T

11740148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134100061-G-C

11740755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134100588-A-G

11740819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134100646-A-G

11740887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134100706-G-T

11740911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134100734-G-T

11741457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134102203-G-C

11741623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134102346-A-G

11741706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134102425-T-C

11741710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134102429-T-C

11742394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134103131-T-G

http://identifiers.org/hco/12/GRCh38#11743199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134104223-C-A

11743199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134104223-C-T

11743316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134104339-G-T

11743357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134104402-C-T

11743390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134104436-T-C

11743402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134104448-G-C

11743403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134104449-G-C

11743432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134104477-G-A

11743477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134104499-G-A

11743477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134104499-G-T

11743756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134104726-A-G

http://identifiers.org/hco/12/GRCh38#11743923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#134104889-C-A

11743923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134104889-C-G

11743923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134104889-C-T

11743944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 134104910-T-C

http://identifiers.org/hco/12/GRCh38#11744026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#134105014-C-A

11744026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134105014-C-T

11744176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134105153-G-A

11744254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134105231-G-A

11744449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134105430-C-T

11744737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134105707-A-G

11744773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134105743-C-T

11744858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134105856-A-T

11744932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134105934-C-G

11744933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134105935-A-G

11744978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134105986-A-G

11745173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134106182-C-T

11745177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134106186-C-T

11745329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134106340-A-G

11745441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134107069-C-G

11745532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134107166-T-C

11745534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134107168-T-C

11746339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134107976-T-A

11746507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134108181-C-G

11746507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134108181-C-T

11746694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134108430-G-A

11746771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134108507-G-T

11746823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134108544-A-T

11746830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134108552-G-T

11747043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134108688-A-T

11747044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134108689-G-C

11747045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134108690-C-T

11747249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134108888-T-C

11747338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134108962-C-T

11747443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134109049-G-A

11747443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134109049-G-C

11747505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134109104-G-A

11747511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134109110-C-G

http://identifiers.org/hco/12/GRCh38#11747527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134109133-C-A

11747570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134109155-G-T

11747767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134109339-C-T

11747773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134109345-C-T

11748201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110108-G-A

11748247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110146-A-G

11748306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110206-G-A

11748382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110266-A-G

11748391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110275-C-G

11748661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110547-T-C

11748685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110563-A-G

11748715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110592-C-T

11748720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110597-T-G

11748735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110612-G-A

11748957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110807-G-A

11748979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110829-C-T

11749010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110855-A-G

11749069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110914-G-C

11749102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110947-G-A

11749117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134110961-G-T

http://identifiers.org/hco/12/GRCh38#11749271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134111112-A-C

11749271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111112-A-G

http://identifiers.org/hco/12/GRCh38#11749353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134111121-C-A

11749354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111122-T-A

11749354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111122-T-C

11749363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111131-T-A

11749363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111131-T-C

11749363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111131-T-G

11749432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111193-C-T

11749611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111383-G-C

11749611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111383-G-T

11749659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111417-C-G

11749660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134111418-T-C

11750190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134111792-G-A

11750414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134111932-G-T

11750500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112011-T-A

11750520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134112036-C-G

11750648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134112163-T-G

11750659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134112174-G-A

http://identifiers.org/hco/12/GRCh38#11750764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134112268-C-A

11750764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112268-C-G

11750764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112268-C-T

11750806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112314-T-C

http://identifiers.org/hco/12/GRCh38#11750860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134112369-C-A

http://identifiers.org/hco/12/GRCh38#11750877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134112385-C-A

http://identifiers.org/hco/12/GRCh38#11750969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134112469-C-A

11750969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112469-C-T

11751055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112557-T-C

11751064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112566-C-T

11751355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112921-T-C

11751369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112934-T-A

11751369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112934-T-G

11751399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112963-G-T

11751413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112977-T-C

11751451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134112998-C-T

11751507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113043-A-T

11751581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113095-G-A

11751599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113113-A-G

11751619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113133-T-A

11751619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113133-T-G

11751686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113198-A-T

11751735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113235-T-C

11751741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113241-G-T

11751746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113246-A-G

11751790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113291-G-T

11751792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113293-G-A

11751792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113293-G-T

http://identifiers.org/hco/12/GRCh38#11751799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134113300-A-C

11751799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113300-A-G

11751799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113300-A-T

11751809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113310-T-C

http://identifiers.org/hco/12/GRCh38#11751814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134113315-A-C

11751814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113315-A-G

11751818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113319-T-A

11751818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113319-T-C

11751884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113374-T-C

11751957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113669-G-A

11751957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134113669-G-T

http://identifiers.org/hco/12/GRCh38#11751965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134113677-C-A

11752259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134114022-C-G

11752408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134114219-G-C

11752408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134114219-G-T

11752595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134114393-C-G

http://identifiers.org/hco/12/GRCh38#11752605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134114403-C-A

11752605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134114403-C-T

11752621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134114412-T-G

11752644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134114439-G-A

11752644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134114439-G-T

http://identifiers.org/hco/12/GRCh38#11752744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134114546-A-C

11752744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134114546-A-G

11752806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134114601-G-A

11752806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134114601-G-T

11752837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134114639-G-A

11752837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134114639-G-T

11752843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134114645-G-T

11752863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134114662-C-G

http://identifiers.org/hco/12/GRCh38#11752871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134114670-C-A

11752920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134114715-C-T

11752923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134114718-T-C

11752943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134114738-C-T

11752977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134114761-G-T

11753832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134115440-C-T

11753854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134115461-T-C

11753874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134115481-T-C

11753885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134115492-T-C

11753902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134115512-A-G

11754036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134115624-A-G

http://identifiers.org/hco/12/GRCh38#11754366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134115877-C-A

11754366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134115877-C-G

11754538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134116037-T-C

11754648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134116135-A-G

11755279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134117685-G-A

11755322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134117722-C-T

http://identifiers.org/hco/12/GRCh38#11755414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134117803-C-A

11755521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134117913-G-A

11755786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134118160-T-C

11755795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134118169-T-C

11755948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134118293-A-G

http://identifiers.org/hco/12/GRCh38#11756126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134118422-A-C

11756175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134118470-G-A

11756424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134118653-T-A

11756424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134118653-T-C

11756447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134118675-G-A

11756476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134118702-G-A

11756659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134118955-C-T

11756716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134119030-C-T

11756827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134119324-T-C

11756828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134119325-C-T

11756831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134119328-G-A

11756831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134119328-G-T

11756832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134119329-C-T

11757098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134119623-A-G

11757098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134119623-A-T

11757413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134119926-A-G

11757563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134120068-T-C

11757815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134120286-T-C

11757899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134120373-T-G

http://identifiers.org/hco/12/GRCh38#11757913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134120387-A-C

11757913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134120387-A-G

http://identifiers.org/hco/12/GRCh38#11757919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134120393-C-A

11758015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134120506-G-T

11758415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134120744-C-T

11758504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134120843-C-G

11758517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134120856-C-T

11758698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134120953-T-C

11759382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134121631-A-G

11759545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134122373-T-C

11759643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134122455-A-G

11759850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134122661-A-G

11759883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134122696-A-G

11759917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134122728-C-T

11760047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134122867-C-T

http://identifiers.org/hco/12/GRCh38#11760053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134122873-C-A

11760112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134122932-A-G

11760217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134123036-C-T

11760425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134123230-A-G

11760521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134123315-A-T

11760854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134123754-A-G

11761023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134123835-A-T

11761044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134123861-C-T

11761046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134123863-G-A

11761137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134123946-C-T

11761244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124080-T-C

11761441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124274-A-G

11761651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124490-A-G

http://identifiers.org/hco/12/GRCh38#11761707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134124535-A-C

11761811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124637-G-A

11761813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124639-T-A

11761813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124639-T-C

http://identifiers.org/hco/12/GRCh38#11761926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134124748-A-C

11761989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124811-A-T

11761995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124817-C-G

11762000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124822-G-A

11762105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124927-G-A

11762105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124927-G-C

11762125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124947-T-G

11762132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134124954-T-C

11762228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125047-C-T

11762295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125114-T-C

11762391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125205-T-G

11762421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125234-C-T

11762445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125264-A-G

11762453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125272-G-A

11762453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125272-G-C

11762453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125272-G-T

11762563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125374-G-A

11762920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125727-A-G

11763044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125825-C-G

11763254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134125960-G-A

11763590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134126453-T-G

11763644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134126566-G-A

11763719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134126623-C-T

11763728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134126632-G-T

11763792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134126699-T-C

11764302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127359-G-A

11764416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127479-A-G

11764416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127479-A-T

11764480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127539-A-G

11764715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127668-G-A

11765133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127988-C-G

11765133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134127988-C-T

11765279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134128140-G-A

11765470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134128324-T-C

11765623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134128452-A-G

11765623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134128452-A-T

11765863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134128710-T-A

11765863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134128710-T-C

11765982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134128837-G-A

11765983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134128838-T-C

11766017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134128873-C-T

http://identifiers.org/hco/12/GRCh38#11766706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134129540-A-C

11766805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134129604-G-C

11766865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134129662-G-C

http://identifiers.org/hco/12/GRCh38#11766936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134129734-A-C

11766968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134129767-G-A

11766968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134129767-G-C

11767353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134130501-G-T

11767470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134130611-G-A

11767775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134131184-A-G

11767802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134131214-G-C

11767917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134131330-A-G

11767946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134131360-G-A

11767946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134131360-G-C

http://identifiers.org/hco/12/GRCh38#11767969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134131383-C-A

11768165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134131532-T-A

11768192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134131549-C-T

http://identifiers.org/hco/12/GRCh38#11768322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134131576-A-C

11768344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134131598-A-G

http://identifiers.org/hco/12/GRCh38#11768376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134131628-C-A

http://identifiers.org/hco/12/GRCh38#11768420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134131672-C-A

http://identifiers.org/hco/12/GRCh38#11768438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134131689-A-C

11768443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134131694-A-T

11768912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134132099-A-G

11768924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134132107-T-C

http://identifiers.org/hco/12/GRCh38#11768932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134132115-C-A

11768932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134132115-C-T

11769053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134132195-G-T

11769109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134132252-G-A

11769161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134132440-C-G

11769207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134132486-C-T

http://identifiers.org/hco/12/GRCh38#11769380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134132638-A-C

11769649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134132880-T-A

http://identifiers.org/hco/12/GRCh38#11769651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134132882-C-A

11769674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134132913-G-C

11769720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134132957-A-G

11769772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133013-G-A

11769772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133013-G-C

11769868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133095-G-A

11769938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133159-C-T

11770202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133363-A-T

11770308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133470-G-T

11770383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133546-A-T

http://identifiers.org/hco/12/GRCh38#11770397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134133561-A-C

11770419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133587-G-C

11770602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133768-A-G

11770603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133769-C-G

11770631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134133785-A-G

11771048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134134148-A-G

11771080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134134169-A-G

11771167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134134253-T-A

11771253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134134327-G-A

11771488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134134620-G-A

11771724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134134857-A-G

11771728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134134861-C-G

11771933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134135018-C-T

http://identifiers.org/hco/12/GRCh38#11772100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134135187-A-C

11772182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134135266-A-G

11772435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134135532-A-G

http://identifiers.org/hco/12/GRCh38#11772521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134135600-C-A

11772609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134135681-A-T

11772631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134135701-A-G

http://identifiers.org/hco/12/GRCh38#11772677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134135747-C-A

11772677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134135747-C-T

11773531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136254-G-A

11773531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136254-G-T

11773583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136311-G-A

http://identifiers.org/hco/12/GRCh38#11773587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134136315-C-A

11773647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136383-G-T

http://identifiers.org/hco/12/GRCh38#11774774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134136690-A-C

11774865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136785-C-T

11774931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136840-C-T

11774981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136872-A-G

11775088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134136982-G-A

11775425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134137543-A-G

11775462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134137580-T-A

11775799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134137900-C-G

11775843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134137938-A-G

11775855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134137949-C-T

11775856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134137950-G-A

11776187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138297-G-A

11776187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138297-G-C

11776194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138304-C-T

11776225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138326-T-G

11776271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134138367-T-C

11777313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134139360-T-C

11777498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134139506-C-T

11777635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134139632-T-C

http://identifiers.org/hco/12/GRCh38#11777773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134139783-A-C

11777958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134139958-T-C

11778004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134140007-C-G

11778507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141317-A-G

11778521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141334-T-C

11778603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141412-A-G

11778814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141745-G-C

11778914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141840-G-A

11779031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134141952-A-T

11779100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142016-C-T

11779145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142059-T-G

11779340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142231-A-G

11779546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142438-T-C

11779551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142443-C-G

11779723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142628-T-C

11780011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142894-G-A

11780011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134142894-G-T

11780157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143165-T-G

11780199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143205-C-G

11780222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143227-T-C

11781048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143599-G-T

11781225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143806-A-G

11781287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134143871-T-A

11781642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134145528-G-C

11782169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146134-C-T

11782345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146258-A-T

11782466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146398-G-C

11782767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134146975-G-A

11783129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134147398-C-T

http://identifiers.org/hco/12/GRCh38#11785523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134148693-A-C

11785593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134148764-A-G

11785596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134148767-T-C

11785656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134148803-G-C

11785702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134148846-A-G

11785761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134148904-A-G

11785805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134148949-T-C

11786005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134149148-T-C

11786126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134149663-T-A

11786256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134149795-T-C

11786354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134149891-C-T

11786602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134150252-C-T

11786654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134150333-C-T

http://identifiers.org/hco/12/GRCh38#11786734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134150456-A-C

11786735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134150457-T-C

11786746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134150468-C-T

11786999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134150706-A-G

11787181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134150864-T-A

11787216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134150896-T-G

11787529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134151354-G-A

11788148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152373-G-T

11788200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152424-G-A

11788250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152474-T-G

http://identifiers.org/hco/12/GRCh38#11788375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134152608-A-C

11788493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152701-T-C

11788522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152730-C-G

11788593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134152768-G-C

http://identifiers.org/hco/12/GRCh38#11788616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134152798-A-C

11791158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134155935-A-G

11791178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134155977-T-A

11791178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134155977-T-C

11791362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156157-A-T

11791376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156171-A-G

11791424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156221-C-T

11791629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156398-A-G

11791640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156409-T-C

11791957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156735-G-A

11791974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156752-G-A

11791974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156752-G-T

11792061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156855-G-A

11792066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134156860-G-A

11792183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134157115-T-C

11792183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134157115-T-G

11792751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134157330-A-G

11792761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134157340-T-C

11792831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134157394-G-A

11792842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134157405-A-G

11792970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134157519-C-T

11793746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159120-G-A

11793778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159140-A-G

11794088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159445-G-A

11794137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159494-G-A

11794313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134159679-C-G

11794659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134160012-C-G

11794748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134160114-C-T

11794994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134160355-A-G

11795195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134160594-A-G

11795212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134160620-A-G

11795284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134160696-G-A

11795301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134160711-G-C

http://identifiers.org/hco/12/GRCh38#11795308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134160718-C-A

11795308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134160718-C-T

11795640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134160944-C-T

11795677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134160981-C-T

http://identifiers.org/hco/12/GRCh38#11795890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134161086-A-C

11795890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134161086-A-G

11796004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134161176-A-G

11796054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134161227-C-T

11796081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134161253-G-A

11796082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134161254-A-T

11796240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134161361-T-G

11796531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134161757-A-G

11796545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134161773-C-T

11796568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134161796-A-G

http://identifiers.org/hco/12/GRCh38#11796579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#134161808-C-A

11796600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134161824-T-C

http://identifiers.org/hco/12/GRCh38#11796622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134161846-C-A

11796742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134161943-A-G

11796742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134161943-A-T

11798159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134162433-A-G

11798181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134162455-C-T

11798456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134162894-G-A

11798536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134162963-G-A

11798908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134163326-C-G

11798995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134163417-C-T

11799401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134163824-C-G

11799440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134163860-C-G

11799444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134163872-T-C

11799565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134164007-G-A

11800482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165127-G-A

11800482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165127-G-T

11800489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165135-A-G

11800621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165409-G-A

11800630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165418-A-G

11800833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165535-C-G

http://identifiers.org/hco/12/GRCh38#11800902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134165612-C-A

11800958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165687-A-G

11800996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165730-C-T

11801162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165896-G-C

11801236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165972-A-G

11801239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134165975-G-A

11801281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134166032-C-T

11801295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134166046-G-C

11801352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134166103-G-A

11801369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134166120-A-G

http://identifiers.org/hco/12/GRCh38#11802031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134166865-C-A

11802119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134166945-G-A

11802144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134166970-A-T

11802395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167172-G-A

11802467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167240-A-G

11802810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167558-G-A

11802810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167558-G-C

11802953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167698-T-C

11802971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167717-T-C

11803220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134167947-A-G

11803316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134168037-C-T

11803403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134168156-T-A

11803403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134168156-T-G

11803428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134168190-G-A

11803516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134168274-G-A

11803669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134168420-C-G

11803940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134168668-T-A

http://identifiers.org/hco/12/GRCh38#11803945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134168673-A-C

11803945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134168673-A-G

11806197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134170087-T-A

11806420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134170335-A-G

11806439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134170354-T-C

11806914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134171198-C-T

11807011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134171284-G-A

11807065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134171338-C-G

11807148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134171420-G-A

11807242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134171681-T-A

11807255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134171694-T-A

http://identifiers.org/hco/12/GRCh38#11807269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134171708-A-C

11807371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134171798-G-C

http://identifiers.org/hco/12/GRCh38#11807724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134172151-C-A

11807787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134172198-A-G

11807950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134172721-G-A

11808021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134172783-A-G

11808075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134172838-A-G

11808216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134172989-C-T

http://identifiers.org/hco/12/GRCh38#11808301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134173075-A-C

11809300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134173301-A-G

11809308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134173309-C-T

11809641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134173603-G-A

11810258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134174030-G-A

11810288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134174064-A-G

11810444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134174249-T-A

11810713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134174841-A-G

11810768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134174893-T-C

11810834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134174954-C-G

11810999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134175057-G-A

11811057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134175081-G-C

11811078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134175100-T-C

11811140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134175151-C-T

11811152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134175163-A-T

11811203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134175202-G-A

11811335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134175341-T-A

11811351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134175358-C-G

11811426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134175433-G-A

11811426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134175433-G-C

11811707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134176139-G-A

11811763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134176198-G-C

11811844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134176266-G-A

11811953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134176371-C-T

11812281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134176697-C-T

11812501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134176884-C-T

11812541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134176926-T-G

11812544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134176929-G-C

11812714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134177034-G-A

http://identifiers.org/hco/12/GRCh38#11812807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134177125-A-C

11812909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134177232-C-T

11812911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134177234-T-C

11812914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134177237-T-C

11813045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134177360-G-A

11813134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134177448-G-A

http://identifiers.org/hco/12/GRCh38#11813257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134177572-C-A

11813257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134177572-C-T

11813266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134177581-C-T

http://identifiers.org/hco/12/GRCh38#11813308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#134177613-C-A

11813360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134177668-G-A

11813670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134177938-A-G

11813671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134177939-T-C

11814336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134178630-T-C

11814351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134178649-A-T

11814360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134178658-T-A

11814479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134178766-C-T

11814554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134178854-G-A

11814627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134178925-G-C

11815080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134179503-G-A

11815715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134179971-C-T

11815724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134179980-G-A

11818553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134181620-A-G

11818759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134181822-C-G

11818759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134181822-C-T

11818792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134181869-A-G

11818896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134181969-C-G

11818896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134181969-C-T

11818983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134182047-C-T

11818996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134182060-C-T

11819009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134182077-C-T

11819013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134182081-G-A

11819014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134182082-T-C

11819060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134182129-T-C

http://identifiers.org/hco/12/GRCh38#11819139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134182246-A-C

11819170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134182292-C-T

11819252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134182376-C-T

11819261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134182381-G-A

11819502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134182785-A-T

11819544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134182818-G-T

11819590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134182856-C-T

11819707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134182944-G-A

11819767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134183005-A-G

11819938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134183183-T-C

11820056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134183294-C-G

11820063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134183301-C-T

11820710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134183979-G-T

11820763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134184047-C-T

11820767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134184052-A-T

11820776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134184064-T-A

11821877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134184569-C-T

11821894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134184602-C-T

11821919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134184627-C-T

11821924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134184637-G-A

11822013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134184693-T-C

11822057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134184738-G-A

11822057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134184738-G-T

11822137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134184808-C-T

11822459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134185131-T-C

11822469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134185141-G-C

11822481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134185153-A-G

11822699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134185360-T-C

11823043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134185698-A-G

11823155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134185801-T-C

11823155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134185801-T-G

http://identifiers.org/hco/12/GRCh38#11823217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134185839-A-C

11823217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134185839-A-G

11823247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134185867-C-T

11823927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134186186-A-G

11824063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134186316-C-T

11824072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134186325-A-G

11824161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134186401-C-G

11824236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134186471-A-G

11824249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134186493-T-A

11824263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134186507-G-C

11824895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134186811-A-T

11825063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134186894-G-A

11825063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134186894-G-T

http://identifiers.org/hco/12/GRCh38#11825143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134186968-C-A

11825143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134186968-C-T

11825159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134186984-C-G

http://identifiers.org/hco/12/GRCh38#11825522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134187249-C-A

11825522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134187249-C-T

11825657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134187398-G-T

11825658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134187399-G-A

11825695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134187431-A-G

11825709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134187445-A-G

11825767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134187501-G-A

11825767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134187501-G-T

http://identifiers.org/hco/12/GRCh38#11826500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134187908-C-A

11826549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134187945-G-T

11826613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 134188005-C-G

11827039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 134188313-T-G

11827168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 134188412-G-T

11827187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 134188437-C-T

http://identifiers.org/hco/12/GRCh38#11827408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134188666-A-C

11827408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 134188666-A-G

http://identifiers.org/hco/12/GRCh38#11827568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134188831-A-C

11827610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134188872-G-A

11827752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134189010-G-A

11827752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134189010-G-C

11827977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134189218-C-T

11828152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134189357-A-G

11828219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134189425-T-C

11828264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134189468-A-G

11828405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134189598-C-T

11828719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134189897-C-T

11830778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134192100-T-C

11831485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134192722-A-G

11831553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134192776-A-G

11831580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134192802-A-G

11831941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134193167-A-G

11832012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134193232-G-A

11832404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134193569-C-G

11832404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134193569-C-T

11832451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134193609-C-G

11832500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134193645-T-C

11832641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134193787-C-T

11832951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134193990-T-C

11833301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134194235-A-G

11833379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134194306-G-A

11833452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134194374-G-A

11833460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134194382-G-A

11833462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134194384-G-A

11833482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134194394-T-G

http://identifiers.org/hco/12/GRCh38#11833488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134194400-C-A

11833489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134194401-A-G

11833557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134194476-G-T

11833615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134194527-C-G

11833671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134194563-A-G

11833701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134194590-G-T

11833710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134194599-A-G

11833738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134194618-C-T

11833818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134194665-G-A

http://identifiers.org/hco/12/GRCh38#11834130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134194933-A-C

11834130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134194933-A-G

11834316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134195153-T-G

11834396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134195234-A-G

11834735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134195659-A-G

11834886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134195817-A-T

11835025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134195954-T-C

11835078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134196007-T-C

http://identifiers.org/hco/12/GRCh38#11835292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134196196-A-C

11835373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134196295-T-C

11835490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134196398-G-C

http://identifiers.org/hco/12/GRCh38#11835861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134196712-A-C

11835861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134196712-A-G

11835883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134196734-C-T

11835931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134196783-T-C

11836218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134197076-A-G

11836638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134197482-G-A

http://identifiers.org/hco/12/GRCh38#11836818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134197664-C-A

11836818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134197664-C-T

http://identifiers.org/hco/12/GRCh38#11836913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134197760-C-A

11836972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134197816-A-G

11837238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134198023-A-G

11837256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134198041-A-T

11837533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134198478-G-A

11837936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134198811-T-C

11837945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134198818-G-A

11838138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134198996-A-G

http://identifiers.org/hco/12/GRCh38#11838155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134199013-C-A

11838294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134199154-C-T

11838378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134199245-C-T

11839022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134199717-G-A

11839022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134199717-G-T

11839061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134199757-A-T

http://identifiers.org/hco/12/GRCh38#11839072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134199769-C-A

11839359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134200036-G-A

11839359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134200036-G-C

11839359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134200036-G-T

http://identifiers.org/hco/12/GRCh38#11844069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134200381-A-C

11844069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134200381-A-G

11844096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134200397-C-G

11844119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134200419-G-A

11844214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134200518-C-T

11844600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134201082-G-C

http://identifiers.org/hco/12/GRCh38#11844718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134201161-C-A

11844802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134201235-G-A

11844802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134201235-G-T

http://identifiers.org/hco/12/GRCh38#11844803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134201236-A-C

11844803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134201236-A-T

11844817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134201250-T-G

http://identifiers.org/hco/12/GRCh38#11845440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134201430-A-C

11845440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134201430-A-G

11845506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134201491-A-T

http://identifiers.org/hco/12/GRCh38#11846226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134202628-A-C

11846226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134202628-A-G

11846731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134203131-A-T

11846741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134203141-C-G

11847012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 134203215-A-G

11847273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134203444-A-G

11847359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134203505-A-T

11847495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134203625-T-C

http://identifiers.org/hco/12/GRCh38#11847525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134203655-A-C

11847583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134203689-A-G

11847590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134203714-G-T

http://identifiers.org/hco/12/GRCh38#11847989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134204109-A-C

11847989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134204109-A-G

11848140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134204241-C-T

11848279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134204361-G-A

11848296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134204378-C-G

11848328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134204409-A-T

11849539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134206089-G-C

11849618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134206156-A-G

11849763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134206299-A-T

11849766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134206302-G-A

11849806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134206343-C-T

11849917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134206449-C-T

11849918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134206450-G-A

http://identifiers.org/hco/12/GRCh38#11849967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134206483-C-A

11849998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134206503-T-G

11850035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134206537-G-A

11850035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134206537-G-T

11850087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134206586-C-T

11850193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134206676-C-G

11850260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134206740-C-T

11850264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134206744-A-G

http://identifiers.org/hco/12/GRCh38#11850444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134206874-A-C

http://identifiers.org/hco/12/GRCh38#11850458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134206888-C-A

11850458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134206888-C-T

11851486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134207898-C-T

11851529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134207936-C-T

11852142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134208537-G-T

http://identifiers.org/hco/12/GRCh38#11852291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134208708-C-A

11852672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134209276-G-C

11853402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134210457-A-G

11853411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134210466-T-C

11853431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 134210486-T-C

11853512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 134210567-C-T

11853617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134210672-T-A

11853617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134210672-T-G

http://identifiers.org/hco/12/GRCh38#11853675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134210730-C-A

11853675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134210730-C-T

11853676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134210731-A-T

11853696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134210751-G-A

11853696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134210751-G-T

11853698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134210753-A-G

11853738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134210777-C-T

11854439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134210925-C-G

11854610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134211060-T-G

11854776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134211215-A-T

11854867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134211301-A-G

11855163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134211400-G-A

11855168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134211405-T-A

11855168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134211405-T-C

11855168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134211405-T-G

11855393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134211496-G-A

11855435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134211555-C-T

11855459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134211583-G-A

11855549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134211658-C-G

11855552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134211661-C-G

11855728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, undefined
orthologous variants: 134211825-A-T

11855737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, undefined
orthologous variants: 134211834-A-T

11855818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134211912-A-G

http://identifiers.org/hco/12/GRCh38#11855982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134212073-C-A

11856239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134212314-C-T

11856338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134212411-G-A

11856473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134212548-T-G

11856474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134212549-G-A

11856764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134212804-G-A

11856857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134212903-T-G

11858274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134213252-C-T

11858301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134213279-C-G

11858370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134213334-A-G

11858376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134213340-G-A

11858376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134213340-G-T

11858517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134213492-T-C

11858649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134213663-G-A

11858762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134213847-G-A

11858916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134213995-G-A

11859028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134214126-C-T

11859697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134214732-A-G

11859727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134214739-T-C

11859763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134214775-A-G

http://identifiers.org/hco/12/GRCh38#11859876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134214881-A-C

11859906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134214911-T-C

11860162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134215351-G-A

11860291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134215518-G-T

11860597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134215724-T-G

http://identifiers.org/hco/12/GRCh38#11860617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134215744-C-A

11860617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134215744-C-T

11860678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134215814-G-A

11860752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134215893-A-T

http://identifiers.org/hco/12/GRCh38#11861040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134216170-C-A

11861835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134216841-A-G

11862146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134217494-C-G

11862192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134217529-A-G

11862294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134217599-G-A

11862554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134217828-G-A

11862554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134217828-G-C

11862653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134217925-A-G

11862688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134217960-G-T

11863535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134220113-C-T

11863740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134220334-G-A

11863806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134220399-C-G

http://identifiers.org/hco/12/GRCh38#11863837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134220427-A-C

11863837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134220427-A-G

11864167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, undefined
orthologous variants: 134220745-A-G

11864317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134220902-A-T

11864581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134221146-G-A

11864594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134221159-C-T

11864599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134221164-A-G

http://identifiers.org/hco/12/GRCh38#11864730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134221355-C-A

11864738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134221363-G-A

11864761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134221386-A-T

11864910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134221539-T-C

11865817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134222443-G-A

11865835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134222461-A-G

http://identifiers.org/hco/12/GRCh38#11865910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134222538-A-C

11865957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134222582-T-C

11866112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134222663-C-G

11866112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134222663-C-T

11866115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134222666-A-T

http://identifiers.org/hco/12/GRCh38#11866170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134222721-C-A

11866170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134222721-C-T

11866439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134222960-G-A

11866455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134222980-T-C

11866463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134222988-G-C

http://identifiers.org/hco/12/GRCh38#11866865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134223367-A-C

11866943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134223440-A-G

11867043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134223516-G-A

11867087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134223553-C-G

11867087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134223553-C-T

11867218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134223697-T-C

http://identifiers.org/hco/12/GRCh38#11867517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134223989-A-C

11867519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134223991-A-G

http://identifiers.org/hco/12/GRCh38#11867525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134223997-A-C

11867525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134223997-A-G

http://identifiers.org/hco/12/GRCh38#11867622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134224096-C-A

11867623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134224097-T-A

11867641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134224111-T-C

11867688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134224157-C-G

11867688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134224157-C-T

11867796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134224254-C-G

11867944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134224400-T-G

11868023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134224464-C-T

11868243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134224663-G-T

11868300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134224708-T-C

11868314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134224722-T-C

11868612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134224795-A-G

11868648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134224831-T-C

11868744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134224893-T-C

11868744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134224893-T-G

11868852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134224992-C-T

11868888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134225028-C-T

11868911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134225051-G-T

http://identifiers.org/hco/12/GRCh38#11869346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134225159-C-A

11869346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134225159-C-T

11869361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134225174-C-T

11869365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134225178-G-C

11869365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134225178-G-T

11869370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134225183-T-A

http://identifiers.org/hco/12/GRCh38#11869372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134225185-C-A

11869388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134225201-C-T

11869389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134225202-T-G

11869455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 134225268-C-T

11869548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 134225361-C-G

11869548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 134225361-C-T

11869599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: synonymous variant
orthologous variants: 134225415-C-T

11869612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: missense variant
orthologous variants: 134225428-G-A

11869612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: missense variant
orthologous variants: 134225428-G-T

11869812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: synonymous variant
orthologous variants: 134225610-C-T

http://identifiers.org/hco/12/GRCh38#11869986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134225786-C-A

11869999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134225802-C-T

11870016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134225819-A-G

11870017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134225820-A-G

11870019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134225822-G-A

11870019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134225822-G-T

http://identifiers.org/hco/12/GRCh38#11870056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134225871-C-A

11870056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134225871-C-T

11870247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134226081-G-A

11870320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134226155-T-C

11870330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134226165-C-T

11870609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134226435-A-G

11870743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134226496-G-C

11870770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134226523-C-G

11870778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134226531-A-G

11870782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134226535-A-G

11871156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134226843-C-T

11871186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134226876-A-G

11871186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134226876-A-T

11871231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134227006-C-T

http://identifiers.org/hco/12/GRCh38#11871232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134227007-A-C

11871249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134227025-C-T

11871250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134227026-G-A

11871294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134227075-T-C

11871619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134227372-A-T

11871635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134227388-G-T

11871708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134227456-A-G

11871775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134227517-A-G

http://identifiers.org/hco/12/GRCh38#11871879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134227604-A-C

11872118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134227792-G-A

11872288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134227922-G-C

11872355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134227987-C-T

http://identifiers.org/hco/12/GRCh38#11872429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134228115-A-C

11872429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134228115-A-T

11872900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134228554-G-A

11872997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134228639-G-T

11873006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134228648-C-T

11873452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134229113-C-T

11873756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134229400-G-T

11875036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134230159-A-G

11875664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134230450-T-C

11875909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134230679-T-C

11875926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134230694-C-T

http://identifiers.org/hco/12/GRCh38#11875960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134230728-A-C

11875962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134230730-G-A

11875962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134230730-G-T

11876014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134230764-G-A

11876023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134230773-G-A

11876196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134230944-G-A

11876250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134230983-G-A

11876623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134231299-C-T

11876711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134231451-A-G

11876814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134231550-G-A

11877580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134232600-A-G

11877672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134232697-G-A

11878269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134233261-A-G

11878452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134233353-C-T

11878642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134233520-T-C

11878676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134233554-C-T

11878702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134233580-C-T

11878767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134233645-C-G

11878894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134233759-G-A

11878936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134233809-G-A

11879192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134234061-C-T

11879687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134234591-G-A

11879781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134235230-C-T

11879856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134235301-T-C

http://identifiers.org/hco/12/GRCh38#11879889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134235334-A-C

11879889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134235334-A-G

11879898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134235343-G-A

11879898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134235343-G-T

11879951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134235396-G-A

11880072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134235498-G-C

11880508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134235942-T-G

11881309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134236470-T-A

11881309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134236470-T-C

11881424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134236584-C-G

11884046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134238292-G-A

11884271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134238500-C-T

http://identifiers.org/hco/12/GRCh38#11884303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134238528-C-A

11884334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134238551-A-G

11884334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134238551-A-T

11884401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134238614-A-G

11884557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 134238765-C-T

11885066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134239264-G-T

11885137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134239338-T-C

11885477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134239607-T-C

11885653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134239715-A-G

http://identifiers.org/hco/12/GRCh38#11885776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134239817-C-A

11885776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134239817-C-T

11885797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134239843-C-G

11885797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134239843-C-T

http://identifiers.org/hco/12/GRCh38#11885798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134239844-C-A

11885882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134239927-G-A

11885882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134239927-G-T

11886080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, undefined
orthologous variants: 134240136-A-G

http://identifiers.org/hco/12/GRCh38#11886112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#134240151-C-A

11886112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron_variant, undefined
orthologous variants: 134240151-C-T

11886195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134240252-T-C

11886235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134240292-C-T

http://identifiers.org/hco/12/GRCh38#11886247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134240300-A-C

http://identifiers.org/hco/12/GRCh38#11886553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134240606-A-C

11886553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134240606-A-G

11886553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134240606-A-T

11886571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134240636-G-A

11886627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134240910-G-A

11886669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134240959-C-T

11886796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134241057-G-A

11886902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134241151-G-A

11887464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134241681-C-T

11887909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134241795-A-G

11887931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134241820-G-A

11887961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134241848-C-T

11887962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134241849-A-G

11888329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134242033-T-C

11890041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134242748-G-C

11890130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134242829-T-C

11890163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134242850-A-G

11890249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134242940-T-C

11890276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134242971-G-T

http://identifiers.org/hco/12/GRCh38#11890891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134243171-C-A

11890901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: intron variant
orthologous variants: 134243181-A-G

11891025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 134243305-A-G

11891170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134243439-A-G

http://identifiers.org/hco/12/GRCh38#11891319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134243585-C-A

11891319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134243585-C-T

11891335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134243606-C-T

11891488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134243782-A-G

http://identifiers.org/hco/12/GRCh38#11891493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134243787-C-A

11891493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 134243787-C-T

11891775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244058-A-G

11891791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244073-C-G

11891791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244073-C-T

11891817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244088-G-A

11891817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244088-G-T

11891853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244113-T-C

11891865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244125-A-G

11892024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244248-G-T

11892140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244343-G-A

11892140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244343-G-T

11892295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244434-G-A

11892317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244456-T-A

11892674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244933-G-A

11892674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244933-G-T

11892704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244964-A-G

11892705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244965-G-T

11892720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134244980-A-G

11892851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245077-A-G

11892853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245079-G-T

11892898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245119-C-G

11892898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245119-C-T

http://identifiers.org/hco/12/GRCh38#11892964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134245155-C-A

11893014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245188-G-C

11893036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245202-G-T

11893198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245344-G-A

11893198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245344-G-T

11893331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245471-G-A

11893331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245471-G-T

11893381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245520-G-T

11893506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245599-G-A

11893506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245599-G-T

11893953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245618-T-C

11894100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245774-G-A

11894100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245774-G-T

11894182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245851-T-C

11894193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245871-G-A

11894195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245873-G-A

11894195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134245873-G-T

11894287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246002-G-T

11894296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246011-T-C

11894382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246094-G-T

11894484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246194-G-A

11894608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246302-T-C

11894616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246310-T-C

11894621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246315-G-C

11894621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246315-G-T

11894628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246322-A-G

11894761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246439-G-T

11894764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246442-A-G

11894808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246482-A-G

http://identifiers.org/hco/12/GRCh38#11894911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134246613-C-A

11894920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246622-A-G

11894934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246636-G-A

11894934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246636-G-C

11895008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134246715-G-T

11895048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134246765-A-G

11895070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: 134246787-G-A

11895207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 134246925-C-T

http://identifiers.org/hco/12/GRCh38#11895300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3495
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134247018-C-A