143407891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42349317-G-A

143407891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42349317-G-T

143408248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42349630-A-G

143408304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42349680-G-T

http://identifiers.org/hco/7/GRCh38#143408578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42349936-C-A

143408578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42349936-C-T

143408616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42349975-T-A

143408616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42349975-T-C

143408786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42350125-A-G

http://identifiers.org/hco/7/GRCh38#143408857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42350195-A-C

143408857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42350195-A-G

143408857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42350195-A-T

http://identifiers.org/hco/7/GRCh38#143409019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42350356-C-A

143409446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42350737-C-G

143409580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42350881-A-G

143409594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42350895-T-A

http://identifiers.org/hco/7/GRCh38#143410461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42351354-A-C

143410461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42351354-A-G

143410461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42351354-A-T

143410463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42351356-G-T

143410701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42351596-G-A

143410715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42351629-C-G

143410724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42351638-C-T

143410837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42351757-A-G

143410843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42351763-C-T

143410898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42351816-G-A

143411087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42351974-T-G

143411159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42352043-C-G

143411159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42352043-C-T

143411400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42352599-T-C

143411496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42352695-G-A

143411592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42352784-G-A

143411697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42352895-C-T

http://identifiers.org/hco/7/GRCh38#143411713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42352907-C-A

143411713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42352907-C-T

143411723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42352917-A-G

143411770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42352964-T-C

143411851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42353051-C-T

143411930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42353128-G-A

143412128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42353292-A-G

http://identifiers.org/hco/7/GRCh38#143413054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42353669-C-A

143413104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42353718-T-C

http://identifiers.org/hco/7/GRCh38#143413189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42353801-C-A

143413650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42354234-G-T

http://identifiers.org/hco/7/GRCh38#143413788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42354378-C-A

143414517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42355019-G-T

143414598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42355119-C-T

143414730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42355161-G-C

143414952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42355414-G-T

143414954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42355416-T-C

http://identifiers.org/hco/7/GRCh38#143414996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42355454-C-A

143415091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42355541-G-A

http://identifiers.org/hco/7/GRCh38#143415104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42355554-A-C

143415121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42355587-G-T

143415141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42355607-A-G

143415153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42355619-A-G

143415164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42355628-A-T

143415371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42355670-T-A

143415374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42355671-T-A

143415374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42355671-T-C

http://identifiers.org/hco/7/GRCh38#143415467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42355760-C-A

143415501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42355803-G-T

143415550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42355852-G-T

143415596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42355893-G-T

143415626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42355921-G-C

143415626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42355921-G-T

http://identifiers.org/hco/7/GRCh38#143415689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42355982-C-A

143415702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42355998-A-G

143415722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42356018-T-C

143415814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42356109-T-C

143415866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42356161-T-C

143415890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42356184-G-A

143415927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42356221-G-A

143416231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42356521-C-T

143416379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42356663-A-G

143416644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42357458-A-G

143416671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42357485-C-T

143416767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42357572-A-G

143416914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42357710-T-C

143416930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42357725-T-C

143416986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42357773-C-G

143417067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42357848-A-G

143417639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42358041-C-T

http://identifiers.org/hco/7/GRCh38#143417781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42358197-A-C

143418143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42358474-C-T

143418188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42358519-T-A

143418188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42358519-T-G

http://identifiers.org/hco/7/GRCh38#143418213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42358530-C-A

143418363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42358682-T-A

143418887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42358933-C-T

143418997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42359048-C-T

143419098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42359121-A-G

143420088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360681-C-T

143420100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360693-G-A

143420134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360727-C-T

143420214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360792-C-T

143420315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360899-G-A

143420315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360899-G-C

143420315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42360899-G-T

143420475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42361063-T-G

143420484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42361072-G-A

143420511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42361099-C-G

143420511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42361099-C-T

143421575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42361456-T-C

http://identifiers.org/hco/7/GRCh38#143421678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42361564-C-A

143421697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42361583-C-T

143421819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42361711-T-C

143421980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42361856-G-A

143421980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42361856-G-T

143422074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42362919-T-G

143422212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42362781-G-T

143422451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42362576-T-C

143422509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42362526-T-C

143425709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42363927-C-T

http://identifiers.org/hco/7/GRCh38#143425871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42364086-C-A

143426069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42364246-G-A

143426507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42364692-T-C

143426622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42364822-T-C

143426825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42364989-T-G

143426906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42365066-A-T

http://identifiers.org/hco/7/GRCh38#143426909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42365069-C-A

http://identifiers.org/hco/7/GRCh38#143426920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42365080-C-A

143426937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42365097-A-G

143428274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42366532-T-C

http://identifiers.org/hco/7/GRCh38#143428397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42366631-C-A

143428897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42366796-G-C

143429133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42367036-G-A

143429335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42367235-C-G

143429335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42367235-C-T

143429944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42367405-G-C

143430094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42367542-T-G

143430317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42367733-G-A

143430546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42367964-A-G

143430652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42368094-A-G

143430947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42368515-G-T

143431123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42368674-T-C

143431140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42368691-G-A

143433169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42370970-G-A

143433211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42371007-G-T

143433444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42371233-C-G

143433444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42371233-C-T

143433523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42371303-A-G

143433827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42372367-T-C

143433860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42372397-G-A

143433935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42372471-G-C

143434228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42372702-C-T

143434322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42372789-A-G

143434396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42372863-C-G

http://identifiers.org/hco/7/GRCh38#143434402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42372869-A-C

143434470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42372932-C-T

143434652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42373097-G-A

143434667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42373291-G-C

143434790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42373434-G-A

143434803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42373440-G-A

143434863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42373506-G-A

143434863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42373506-G-T

http://identifiers.org/hco/7/GRCh38#143435009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42373654-A-C

http://identifiers.org/hco/7/GRCh38#143435010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42373655-A-C

143435363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42373822-T-G

143435429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42373886-G-A

143435510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42373963-G-A

143435529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42373982-T-A

143435537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42373990-T-C

143435550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42374003-G-A

143436241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42374377-T-G

143436825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42376981-A-G

143437085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377222-A-G

143437137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377274-T-C

143437157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377294-G-A

143437157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377294-G-T

143437158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377295-T-C

http://identifiers.org/hco/7/GRCh38#143437159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42377296-C-A

143437159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377296-C-G

http://identifiers.org/hco/7/GRCh38#143437192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42377329-C-A

143437192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377329-C-T

http://identifiers.org/hco/7/GRCh38#143437196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42377333-C-A

143437325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377462-G-A

143437325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377462-G-T

143437385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377522-G-A

143437385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377522-G-T

143437469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377606-T-G

http://identifiers.org/hco/7/GRCh38#143437502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42377639-C-A

143437573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377707-A-G

143437676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377813-G-A

143437676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377813-G-T

http://identifiers.org/hco/7/GRCh38#143437748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42377885-C-A

143437798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377935-A-G

143437832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377966-G-C

143437832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377966-G-T

http://identifiers.org/hco/7/GRCh38#143437844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42377978-C-A

143437844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42377978-C-T

143437956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42378082-G-A

143437956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42378082-G-T

143437998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42378124-G-T

143438069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42378147-T-C

143439143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42379283-G-A

143439145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42379285-A-T

143440997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42380207-C-T

143442884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42381923-G-A

143442884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42381923-G-T

143442963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42381998-A-T

143443133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42382178-T-A

143443133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42382178-T-C

http://identifiers.org/hco/7/GRCh38#143443327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42382377-C-A

143443327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42382377-C-T

143443357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42382407-G-A

143443357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42382407-G-T

143443360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42382410-G-A

143443360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42382410-G-T

http://identifiers.org/hco/7/GRCh38#143443413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42382455-A-C

http://identifiers.org/hco/7/GRCh38#143443435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42382472-A-C

143443444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42382481-A-G

http://identifiers.org/hco/7/GRCh38#143443509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42382546-C-A

143443509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42382546-C-T

143443967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42383004-G-A

143443978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42383015-C-T

143444052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42383089-T-G

143444067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42383104-C-T

143444104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42383141-A-G

143444178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42383215-C-T

http://identifiers.org/hco/7/GRCh38#143444239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42383276-C-A

143444396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42383433-G-A

143444396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42383433-G-T

http://identifiers.org/hco/7/GRCh38#143444404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42383441-C-A

143444404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42383441-C-T

143444413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42383450-A-G

143444467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42383478-G-A

143444467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42383478-G-T

143444468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42383479-G-A

143444468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42383479-G-T

http://identifiers.org/hco/7/GRCh38#143444950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42383792-C-A

143445304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42384135-C-T

143445418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42384253-G-T

143445590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42384414-C-T

143445651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42384465-C-T

143445723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42384528-G-A

http://identifiers.org/hco/7/GRCh38#143446043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42384709-C-A

http://identifiers.org/hco/7/GRCh38#143447191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42387207-C-A

143447191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42387207-C-T

143447234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42387255-G-C

143447234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42387255-G-T

143447245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42387266-A-G

http://identifiers.org/hco/7/GRCh38#143447409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42387455-C-A

143447420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42387466-T-C

143447497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42387539-G-A

143450617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42389738-A-G

143451542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42390797-G-A

143451883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42391099-C-T

143451978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42391203-C-G

143452012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42391237-C-T

143452109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42391323-A-G

143452110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42391324-T-C

143452433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42391823-G-A

143452490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42391878-T-C

143452990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392237-G-A

143453018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392266-A-T

143453052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392294-G-A

143453052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392294-G-T

143453076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392300-G-C

143453171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392403-T-C

143453304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392525-T-C

143453315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392536-G-T

http://identifiers.org/hco/7/GRCh38#143453360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42392572-C-A

143453360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392572-C-G

143453360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392572-C-T

143453391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392603-C-T

143453922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392779-A-G

143453945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392819-G-A

143453952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392826-T-C

143453987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42392861-A-G

143454364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42393225-A-G

143454689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42393610-T-C

143454690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42393611-G-T

143454948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42393849-G-A

143455051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42393979-G-A

143455064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42393992-C-T

143455077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42394005-A-G

143455302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42394835-G-A

143455611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42395134-A-G

143455770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42395310-G-C

143456490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42396043-A-G

143457373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42397849-A-G

143457430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42397906-C-T

143457543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42398073-C-T

143458063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42398306-G-A

143458063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42398306-G-T

143458117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42398350-A-G

http://identifiers.org/hco/7/GRCh38#143458159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42398390-C-A

143458239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42398467-C-G

143458302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42398518-C-T

143458438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42398651-C-T

143458530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42398746-G-C

143458586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42398803-C-T

143459978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42399695-A-G

http://identifiers.org/hco/7/GRCh38#143460249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42399977-A-C

143460438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42400149-G-A

143461512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42400598-A-G

http://identifiers.org/hco/7/GRCh38#143461747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42400825-C-A

143461747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42400825-C-T

143462673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42400954-A-G

143462769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42401045-G-A

143464440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42401758-G-A

143464440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42401758-G-T

143466810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42402349-A-T

143466855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42402392-A-G

143467053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42402578-A-G

143467253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42402737-T-A

143467307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42402795-C-G

143467372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42402846-A-G

143467389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42402863-T-G

143467541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42402978-A-G

143467611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403058-G-A

143468266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403738-G-T

143468296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42403766-T-G

143469218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404016-T-C

143470166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42404927-C-T

143470250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42405010-G-A

143470306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42405063-C-G

143470334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42405091-T-C

143470715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42405443-C-T

143470718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42405446-G-A

143470975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42405782-A-G

143471130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42406150-C-G

143471130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42406150-C-T

143471180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42406197-T-A

143471353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42406363-A-T

http://identifiers.org/hco/7/GRCh38#143471357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42406367-A-C

143471359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42406369-C-T

143471395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42406404-T-C

143471411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42406420-T-A

143471428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42406437-T-C

http://identifiers.org/hco/7/GRCh38#143471568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42406556-A-C

143471652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42406634-A-G

143476317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42409870-A-G

143476392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42409945-T-C

143476524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42410085-C-T

143476533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42410094-T-A

143476539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42410096-G-A

143476648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42410205-A-G

143476899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42410442-A-G

143477064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42410653-A-G

143477350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42410901-G-C

143477360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42410911-C-T

143477742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42411340-G-A

143477742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42411340-G-T

143477748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42411346-G-T

143477885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42411481-C-T

143478059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42411655-A-G

143478064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42411660-G-A

143478086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42411682-C-T

143478286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42411882-C-T

143478486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42412085-A-G

143478486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42412085-A-T

http://identifiers.org/hco/7/GRCh38#143478523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42412122-C-A

143478523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42412122-C-T

143478541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42412140-C-T

143478594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42412193-T-G

http://identifiers.org/hco/7/GRCh38#143478809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42412408-C-A

143478809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412408-C-G

143478820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412419-C-T

143478840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412441-G-A

http://identifiers.org/hco/7/GRCh38#143478865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42412472-C-A

143478865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412472-C-T

143478899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412502-G-A

143478899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412502-G-C

143478899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412502-G-T

http://identifiers.org/hco/7/GRCh38#143478919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42412522-C-A

143479004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412591-T-C

143479005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412592-G-A

143479104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412682-G-A

143479195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412768-G-A

143479249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42412821-G-T

http://identifiers.org/hco/7/GRCh38#143479426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42413006-A-C

143479487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42413048-C-G

http://identifiers.org/hco/7/GRCh38#143479603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42413195-A-C

143480148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42413599-C-T

143480225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42413685-C-G

143480324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42413778-T-G

143480385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42413841-G-A

143480547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42413992-C-G

143481716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42424917-C-G

143481929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42425121-G-A

143482242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42425898-C-T

143482258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42425914-C-G

143482360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42426010-C-T

143482450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42426102-C-T

143487698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42436230-G-A

143488033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42436522-T-G

143488090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42436569-T-C

http://identifiers.org/hco/7/GRCh38#143488346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42436851-C-A

143488346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42436851-C-G

143488346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42436851-C-T

http://identifiers.org/hco/7/GRCh38#143488347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42436852-A-C

143488347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42436852-A-G

143488350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42436855-C-T

143488361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42436866-G-A

143488361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42436866-G-C

143488361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42436866-G-T

143488367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42436872-A-G

143488380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42436885-T-C

143488380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42436885-T-G

http://identifiers.org/hco/7/GRCh38#143488428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42436979-C-A

143488461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42437009-T-C

http://identifiers.org/hco/7/GRCh38#143488462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42437010-C-A

143488462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437010-C-T

143488504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437052-A-G

http://identifiers.org/hco/7/GRCh38#143488510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42437058-C-A

143488510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437058-C-T

143488540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437088-G-A

143488540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437088-G-C

143488540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437088-G-T

http://identifiers.org/hco/7/GRCh38#143488564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42437112-C-A

143488564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437112-C-T

143488631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437179-G-A

143488631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437179-G-C

143488631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437179-G-T

http://identifiers.org/hco/7/GRCh38#143488786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42437334-C-A

143488786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437334-C-T

143488870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437418-G-A

143488870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437418-G-T

143488903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437451-G-T

143488911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437459-G-A

143488911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437459-G-T

http://identifiers.org/hco/7/GRCh38#143488977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42437525-C-A

143488977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437525-C-T

143488986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437534-G-A

143488986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437534-G-C

143488986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437534-G-T

http://identifiers.org/hco/7/GRCh38#143488999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42437547-C-A

143488999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437547-C-T

http://identifiers.org/hco/7/GRCh38#143489012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42437560-C-A

143489035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437583-G-A

143489035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437583-G-T

143489038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437586-G-A

http://identifiers.org/hco/7/GRCh38#143489110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42437658-C-A

143489110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437658-C-T

143489169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437718-G-A

143489169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437718-G-T

http://identifiers.org/hco/7/GRCh38#143489172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42437721-C-A

143489172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437721-C-T

143489235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437784-G-T

143489250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437799-C-G

143489250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437799-C-T

143489268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437817-G-T

143489309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42437858-C-T

143489461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42438120-T-C

http://identifiers.org/hco/7/GRCh38#143489550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42438206-C-A

143489550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42438206-C-T

143489580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42438235-G-A

143489605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42438259-A-G

143489718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42438410-T-C

143489739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42438431-G-A

143489809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42438499-T-C

143489813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42438503-G-C

143490001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42438671-C-T

143490267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42438906-C-G

143490331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42438972-G-C

143490439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42439081-C-T

143490519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42439147-T-G

143490581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42439198-T-C

143490915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42439535-A-G

143490928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42439548-G-T

143491239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42467057-G-C

143491241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42467059-C-T

143491385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42467163-C-T

143491421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42467194-G-A

143491448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42467228-G-A

143491448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42467228-G-C

143491634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42467405-A-G

143491661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42467659-T-C

http://identifiers.org/hco/7/GRCh38#143491681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42467679-C-A

143491778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42467776-T-C

143491952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42467936-A-G

143491981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42467965-G-A

http://identifiers.org/hco/7/GRCh38#143492337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42468325-A-C

143492480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42468451-A-T

143492506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42468477-A-G

143492521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42468492-T-C

143492596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42468559-A-G

143492608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42468572-G-A

143492631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42468596-G-A

143492673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42468636-G-C

143493150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42469011-C-G

143493404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42469199-G-A

143493404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42469199-G-T

http://identifiers.org/hco/7/GRCh38#143493428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42469222-C-A

143493478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42469275-G-T

143493898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42477388-T-A

143494029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42477504-G-A

143494029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42477504-G-C

143494149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42477626-T-C

143494389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42477977-A-G

143494423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42478016-T-C

143494646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42478199-G-T

143494701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42478249-A-G

143494701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42478249-A-T

143494815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42478354-T-C

143495624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42480049-C-T

143496197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42480617-A-G

143496631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42483406-A-G

143497068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42483938-A-G

143497159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42484029-A-G

http://identifiers.org/hco/7/GRCh38#143497270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42484136-C-A

143497270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42484136-C-T

143497323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42484187-T-C

143497349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42484218-G-A

143497863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42484717-C-T

143498643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42486454-T-C

143499243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42486716-A-G

143499367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42486831-C-T

http://identifiers.org/hco/7/GRCh38#143499497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42486941-C-A

143499597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42487034-A-G

143499767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42486514-G-A

143499798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42486483-C-T

143499827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42486454-A-G

143499919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42486366-G-A

143500743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42490186-G-A

143500814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42490253-G-C

http://identifiers.org/hco/7/GRCh38#143500917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42490344-C-A

143500955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42490386-G-C

143501110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42490480-C-G

143501477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42490826-C-T

143501497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42490846-C-T

143501499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42490848-G-C

143501587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42490934-A-G

143501627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42490974-T-C

143502397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42493586-C-G

143502770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42493668-T-A

143502770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42493668-T-C

http://identifiers.org/hco/7/GRCh38#143502817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42493713-C-A

143502817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42493713-C-T

143502931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42493799-T-C

143503034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42493898-A-G

143503035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42493899-C-T

143503108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42493972-C-T

143503491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42494610-G-A

http://identifiers.org/hco/7/GRCh38#143503705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42495218-C-A

143503706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42495219-T-C

143503733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42495243-A-T

143503826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42495338-G-A

143503888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42495403-T-A

143503888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42495403-T-C

143503959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42495471-C-T

143504221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42495669-C-T

143504260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42495704-A-G

http://identifiers.org/hco/7/GRCh38#143504465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42495848-C-A

143504672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42496020-C-T

http://identifiers.org/hco/7/GRCh38#143504797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42496139-C-A

143504804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42496146-A-G

143504804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42496146-A-T

143504832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non_coding_transcript_variant, undefined
orthologous variants: 42496174-T-C

143504892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42496227-G-T

http://identifiers.org/hco/7/GRCh38#143504919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42496254-C-A

143504919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42496254-C-T

143504939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42496272-G-A

143504939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42496272-G-C

143504939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42496272-G-T

143505353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42497539-T-C

143505354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42497540-G-T

143505455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42497652-A-G

143505605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42497785-G-T

143506196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42497967-C-T

143506299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42498050-T-A

143506335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42498087-G-A

143506608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42498555-G-A

143506646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42498590-G-T

143506800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42498723-C-T

143507305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42499086-G-A

143507548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42499264-T-A

143507553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42499269-C-T

143507665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42499380-T-C

143507699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42499413-A-G

http://identifiers.org/hco/7/GRCh38#143508047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42499758-C-A

143508047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42499758-C-T

143508185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42499802-A-G

143508201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42499818-G-A

143508229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42499846-G-A

143508229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42499846-G-T

143508581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42500083-G-A

143508641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42500143-C-T

143508765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42500281-T-C

http://identifiers.org/hco/7/GRCh38#143508816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42500332-C-A

143508816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42500332-C-T

143508875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42500391-C-T

143508903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42500419-G-T

143508925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42500441-T-G

143508933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42500475-G-T

143509083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42500850-T-C

143509083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42500850-T-G

143509292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42501119-C-T

143509335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42501158-G-A

143509395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42501217-G-T

143509411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42501233-C-G

143509440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42501273-T-C

http://identifiers.org/hco/7/GRCh38#143509457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42501291-C-A

143509470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42501304-G-T

http://identifiers.org/hco/7/GRCh38#143509483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42501317-C-A

143509483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42501317-C-T

143509582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42501414-G-A

143509582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42501414-G-C

143509597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42501429-A-G

143509647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42501540-T-C

143509662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42501565-G-A

143510482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42502487-G-T

143510503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42502510-T-C

143510504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42502511-G-T

143510555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42502561-C-G

http://identifiers.org/hco/7/GRCh38#143510585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42502590-C-A

143510585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42502590-C-T

143510598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42502603-G-T

143510852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42514910-G-A

143510885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42514944-A-G

143510897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42514957-G-A

143510897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42514957-G-T

143510909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42514969-C-T

http://identifiers.org/hco/7/GRCh38#143510926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42514987-C-A

143510926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42514987-C-T

143511101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515145-G-A

143511101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515145-G-C

143511170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515214-C-T

143511175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515219-C-T

143511290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515334-G-A

143511290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515334-G-T

http://identifiers.org/hco/7/GRCh38#143511311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42515355-C-A

143511311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515355-C-T

http://identifiers.org/hco/7/GRCh38#143511350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42515394-C-A

143511350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515394-C-T

143511413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515457-G-A

143511413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515457-G-C

143511428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515472-C-T

143511449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515493-G-C

143511449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515493-G-T

http://identifiers.org/hco/7/GRCh38#143511484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42515528-C-A

143511484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515528-C-G

143511484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515528-C-T

143511560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515604-G-A

143511560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515604-G-T

143511616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515660-G-A

143511616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515660-G-T

143511620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515664-G-A

143511620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515664-G-T

143511638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515682-G-A

143511638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515682-G-T

http://identifiers.org/hco/7/GRCh38#143511756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42515799-C-A

143511756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515799-C-T

http://identifiers.org/hco/7/GRCh38#143511767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42515810-C-A

143511767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515810-C-T

143511794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515837-G-T

143511799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515842-G-A

143511799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515842-G-T

143511929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42515970-G-A

http://identifiers.org/hco/7/GRCh38#143512072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42516096-C-A

143512072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42516096-C-T

143512179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42516190-C-T

143512321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42516358-A-G

http://identifiers.org/hco/7/GRCh38#143512406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42516445-C-A

143512641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42516709-T-G

143512674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42516742-G-A

143512747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42516813-T-C

143512770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42516828-G-A

143513127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42517176-A-G

143513151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42517201-G-A

143514918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518366-A-G

143514947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42519464-C-T

143515246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42519753-C-G

143515461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42519973-C-T

143515622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42520161-C-T

143515941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42520614-C-T

143515949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42520622-T-A

143515960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42520633-T-C

143516056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42520694-T-C

143516091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42520732-G-A

143516452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42521091-T-C

143517476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42522270-G-A

143517476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42522270-G-C

143517588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42522371-A-G

143517769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42522614-A-T

143518119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42522968-C-T

http://identifiers.org/hco/7/GRCh38#143518134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42522982-A-C

143518438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42523297-A-G

143518464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42523323-G-T

143518536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42523363-G-A

143518557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42523377-C-T

143518650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42523480-A-G

http://identifiers.org/hco/7/GRCh38#143518836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42523651-C-A

http://identifiers.org/hco/7/GRCh38#143519148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42523937-C-A

143519148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42523937-C-T

http://identifiers.org/hco/7/GRCh38#143519165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#42523954-C-A

143519165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 42523954-C-T

143519265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 42524056-G-T

143519371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42524156-C-T

143519436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 42524213-G-A

http://identifiers.org/hco/7/GRCh38#143519583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42524376-C-A

143519583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42524376-C-T

143519684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42524478-G-T

143519721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42524515-G-T

http://identifiers.org/hco/7/GRCh38#143519808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42524598-C-A

143519813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42524603-G-A

143519813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42524603-G-T

http://identifiers.org/hco/7/GRCh38#143519858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42524646-C-A

143519926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42524715-G-A

143519926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42524715-G-T

http://identifiers.org/hco/7/GRCh38#143519983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42524770-C-A

143520088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42524879-A-G

http://identifiers.org/hco/7/GRCh38#143520097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42524888-C-A

143520130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42524943-G-A

143520175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42524990-A-G

143520358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525184-T-C

143520544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525352-G-T

143520634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525425-G-T

143520641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525432-G-A

143520641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525432-G-T

143520656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525451-G-A

143520656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525451-G-T

143520757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525525-G-T

143520781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525547-A-G

http://identifiers.org/hco/7/GRCh38#143520814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42525567-A-C

143520814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525567-A-G

143520957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525718-C-T

143520966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525726-T-C

143521038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525796-G-T

143521041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525799-G-T

http://identifiers.org/hco/7/GRCh38#143521112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42525823-C-A

143521112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525823-C-T

143521201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525908-A-G

143521210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42525917-C-T

143521725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42526010-A-G

143521779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42526049-G-A

143521779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42526049-G-T

http://identifiers.org/hco/7/GRCh38#143522394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42527057-C-A

143522518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42527180-C-T

143522563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42527225-C-T

143522659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42527325-G-T

http://identifiers.org/hco/7/GRCh38#143522665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#42527331-C-A

143522665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42527331-C-T

143522673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42527339-T-C

143522679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42527353-T-C

143522680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42527354-G-A

143522680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42527354-G-T

143522763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42527441-G-T

143522824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42527493-C-T

143522883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42527538-C-T

143522948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42527578-A-T

143522955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42527585-T-A

143522959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27799
most severe consequence: non coding transcript exon variant
orthologous variants: 42527589-G-A