140401858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 36693681-G-A

140401942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5 prime UTR variant
orthologous variants: 36693765-A-G

140402163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 36693986-A-G

140402222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 36694057-G-A

140402222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 36694057-G-T

http://identifiers.org/hco/5/GRCh38#140402355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36694188-C-A

140402355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36694188-C-T

140402480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36694321-G-A

140403333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, undefined
orthologous variants: 36695019-A-G

140403498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36695112-G-A

140405241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36696424-T-A

140406943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, undefined
orthologous variants: 36697926-T-A

140408005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36699226-T-A

140423298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36703801-T-G

140423434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36703930-G-C

140435204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36707300-C-T

140435253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36707344-T-G

http://identifiers.org/hco/5/GRCh38#140436034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36708002-C-A

140436034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36708002-C-T

http://identifiers.org/hco/5/GRCh38#140436051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36708019-C-A

140436051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36708019-C-T

140436379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36708444-T-G

140438006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36711242-G-A

140438754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36711915-A-G

140438766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36711927-G-A

140439017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36712653-T-C

140440110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36714112-T-C

http://identifiers.org/hco/5/GRCh38#140440334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36714436-C-A

140440334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36714436-C-T

140440608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36715736-A-G

140440843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36716527-G-T

http://identifiers.org/hco/5/GRCh38#140440912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36716593-C-A

140440912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36716593-C-T

140441892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36717739-A-G

140441999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36717838-T-G

140445722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36722381-T-C

140446266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36722917-A-G

140448439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36723908-G-A

140448702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36724147-C-G

140448748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36724194-C-T

140448958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36724380-A-G

140449177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36724476-G-T

http://identifiers.org/hco/5/GRCh38#140458538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36727076-C-A

140458538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36727076-C-T

140458795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36727308-A-G

140458795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36727308-A-T

140459045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36727747-T-A

140459045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36727747-T-G

http://identifiers.org/hco/5/GRCh38#140459050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36727752-C-A

140459050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36727752-C-T

140459052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36727754-G-A

140459052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36727754-G-C

140459052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36727754-G-T

140459089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36727789-A-G

140459089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36727789-A-T

140459129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36727822-T-C

140459479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36728176-G-A

140459479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36728176-G-T

140464465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36733601-G-A

140464510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36733646-A-G

http://identifiers.org/hco/5/GRCh38#140464867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36734012-C-A

140464867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36734012-C-T

140464888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36734046-T-A

140464926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36734182-T-G

140464927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36734183-T-A

140464933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36734189-T-A

http://identifiers.org/hco/5/GRCh38#140464957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36734257-C-A

http://identifiers.org/hco/5/GRCh38#140464977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36734277-C-A

140465317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36734773-G-A

140465317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36734773-G-T

140465657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36735026-T-C

140471452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36740090-A-G

http://identifiers.org/hco/5/GRCh38#140472523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36741186-C-A

140482794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36745030-T-C

140483063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36745261-G-A

140483063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36745261-G-T

140483943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36745635-T-C

140483954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36745647-A-T

140484056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36745759-A-G

140484923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36745965-A-G

140484923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36745965-A-T

http://identifiers.org/hco/5/GRCh38#140484941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36745983-C-A

140484941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36745983-C-T

http://identifiers.org/hco/5/GRCh38#140484991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36746028-C-A

140484991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36746028-C-G

http://identifiers.org/hco/5/GRCh38#140485376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36746569-A-C

140485376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36746569-A-G

140485714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36747011-T-C

140485738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36747035-G-A

140486562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36747119-A-G

http://identifiers.org/hco/5/GRCh38#140486786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36747363-A-C

140486786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36747363-A-G

140487032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36747842-C-T

140487234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36748045-A-G

140487329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36748140-A-G

140487329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36748140-A-T

140488090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36749426-T-C

140488090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36749426-T-G

140489706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36750284-T-A

140493467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36753080-T-A

140493605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36753197-T-C

140493855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36753809-A-G

140494488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36754209-T-A

140494939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36755197-G-A

140496148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36756315-A-G

140496436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36757384-T-A

140496440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36757388-T-C

140496440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36757388-T-G

140496444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36757485-T-C

140497028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36758070-G-A

140499163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36759885-A-G

140499240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36759955-G-T

140499422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36760111-C-G

140499489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36760165-G-A

140499734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36760439-C-T

140499887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36760591-G-T

http://identifiers.org/hco/5/GRCh38#140500216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36760924-A-C

http://identifiers.org/hco/5/GRCh38#140500630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36761298-C-A

140500647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36761315-T-A

140500647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36761315-T-C

140500647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36761315-T-G

140501872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36762884-C-T

140503468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36764099-C-G

140503468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36764099-C-T

140503538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36764156-A-T

140503738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36764308-T-C

140504798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36765097-G-A

140505058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36765354-T-A

140505577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36765651-T-C

140505696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36765733-T-C

140506545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36766569-G-A

140506572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36766595-G-A

140507682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36767538-G-A

140507750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36767611-T-C

140507775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36767636-C-T

140507863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 36767723-C-T

140508011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36767872-T-C

http://identifiers.org/hco/5/GRCh38#140508113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36767935-A-C

140508113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36767935-A-G

140508113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36767935-A-T

140508329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36768145-G-A

140508333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36768149-T-A

140509619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36771240-A-G

http://identifiers.org/hco/5/GRCh38#140509648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36771269-C-A

140509648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36771269-C-T

140509809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 36771430-A-G

140509809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 36771430-A-T

http://identifiers.org/hco/5/GRCh38#140509912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36771515-A-C

140510267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36771855-T-C

140510267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36771855-T-G

140510679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36772257-G-A

140510679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36772257-G-C

140512705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36773094-G-C

140512705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36773094-G-T

http://identifiers.org/hco/5/GRCh38#140512744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36773142-C-A

http://identifiers.org/hco/5/GRCh38#140512798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36773234-C-A

http://identifiers.org/hco/5/GRCh38#140512804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36773273-C-A

140512804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36773273-C-T

140512966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36773456-G-A

140512966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36773456-G-T

140513505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36774771-T-C

140524532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36776686-T-G

140524723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36776818-G-C

http://identifiers.org/hco/5/GRCh38#140526333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36777651-A-C

140526367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: missense variant
orthologous variants: 36777685-T-A

140526450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 36777774-T-G

http://identifiers.org/hco/5/GRCh38#140526477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36777801-C-A

140526477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36777801-C-T

http://identifiers.org/hco/5/GRCh38#140527092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36778310-C-A

140527092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36778310-C-T

140527259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36779051-A-T

140527284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36779073-T-G

http://identifiers.org/hco/5/GRCh38#140527540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36779322-C-A

140527870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 36779741-T-C

140527909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: synonymous variant
orthologous variants: 36779780-G-A

140527978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: synonymous variant
orthologous variants: 36779849-G-T

140528069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36779940-G-A

140528069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36779940-G-C

140528072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36779943-G-A

http://identifiers.org/hco/5/GRCh38#140528128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36780071-C-A

140528128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36780071-C-T

140528208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: synonymous variant
orthologous variants: 36780208-T-C

140528400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: synonymous variant
orthologous variants: 36780400-G-A

http://identifiers.org/hco/5/GRCh38#140528478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36780478-A-C

140528478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: synonymous variant
orthologous variants: 36780478-A-G

140528737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: missense variant
orthologous variants: 36780737-G-A

140528757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: synonymous variant
orthologous variants: 36780757-C-G

140528757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: synonymous variant
orthologous variants: 36780757-C-T

140528880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: synonymous variant
orthologous variants: 36780880-T-A

140528933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: missense variant
orthologous variants: 36780933-G-C

140529099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: synonymous variant
orthologous variants: 36781096-C-T

140529237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: synonymous variant
orthologous variants: 36781234-A-G

140529708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36781705-G-A

140530851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36784214-A-G

140534839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36786474-A-G

140534888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36786709-C-T

140535225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36787040-T-C

140535553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36787334-G-A

http://identifiers.org/hco/5/GRCh38#140535953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36787525-A-C

140535969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36787538-T-G

140536015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36787580-G-T

140536043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36787608-T-G

140536046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36787611-G-A

140536703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36788173-T-G

140537516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36788657-C-G

140537516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36788657-C-T

140537553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36788694-A-G

http://identifiers.org/hco/5/GRCh38#140537708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36789286-C-A

140537708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36789286-C-G

http://identifiers.org/hco/5/GRCh38#140537801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36789366-C-A

140537801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36789366-C-G

140537801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36789366-C-T

140538056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36789709-T-C

140538414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36790062-C-T

140538477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36790124-C-G

http://identifiers.org/hco/5/GRCh38#140538782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36790908-C-A

140538846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron variant
orthologous variants: 36790966-G-A

140539032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 36791140-C-T

140539259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36791353-C-T

140539274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36791368-G-A

140539274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36791368-G-T

140539314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36791408-A-G

140539495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36791604-G-A

140539495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36791604-G-T

http://identifiers.org/hco/5/GRCh38#140539590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36791703-C-A

http://identifiers.org/hco/5/GRCh38#140539662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#36791774-C-A

140539662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36791774-C-T

140539669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36791781-G-A

140539669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36791781-G-T

140539790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24714
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36791902-A-T