http://identifiers.org/hco/5/GRCh38#321801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74440366-C-A

321801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74440366-C-T

http://identifiers.org/hco/5/GRCh38#321816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74440351-C-A

321816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74440351-C-G

http://identifiers.org/hco/5/GRCh38#321850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74440317-C-A

321850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74440317-C-T

321861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74440307-G-A

321861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74440307-G-T

http://identifiers.org/hco/5/GRCh38#322019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74440182-C-A

322097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74440093-T-A

322097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74440093-T-G

325020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74438344-G-A

325346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74438035-G-A

325357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74438024-G-A

341712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74432676-T-C

342153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74432311-C-T

342217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74432245-T-C

342773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74431790-A-G

342941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74431647-G-C

343013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74431575-G-A

http://identifiers.org/hco/5/GRCh38#343910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74431208-C-A

http://identifiers.org/hco/5/GRCh38#348197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74429122-C-A

348262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74429054-C-T

349798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74428800-A-G

349922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74428708-G-A

349922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74428708-G-T

349923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74428707-A-T

350069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74428566-G-C

350246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74428452-A-G

350791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74427850-A-G

350848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74427813-G-A

350991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74427705-C-G

351275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74427435-T-C

351317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74427393-C-T

351520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74427206-T-G

351567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74427150-G-A

351621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74427095-T-C

351732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74426989-T-C

353263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74426330-G-C

353372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74426224-C-T

353425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74426174-G-A

353425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74426174-G-T

353471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74426126-T-C

353471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74426126-T-G

353552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74426074-C-T

http://identifiers.org/hco/5/GRCh38#353689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74425965-C-A

353689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74425965-C-T

353776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74425880-C-T

http://identifiers.org/hco/5/GRCh38#353933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74425724-A-C

353955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74425697-G-A

353955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74425697-G-T

354882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74424498-C-T

354956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74424432-C-T

http://identifiers.org/hco/5/GRCh38#355016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74424357-C-A

355016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74424357-C-T

355393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74423993-C-T

355394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74423992-G-A

355567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74423360-C-T

355705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74423201-C-G

http://identifiers.org/hco/5/GRCh38#356150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74422613-C-A

356150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74422613-C-T

356362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74422424-G-A

356475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74422319-G-A

http://identifiers.org/hco/5/GRCh38#359419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74422280-C-A

359480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74422215-C-T

359618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74422072-C-T

359801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74421886-A-G

359808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74421879-G-A

http://identifiers.org/hco/5/GRCh38#359883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74421769-C-A

360064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74421589-G-A

360085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74421568-G-C

360315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74421403-G-T

360411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74421313-G-A

360820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74420920-A-G

362930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74419777-C-T

364776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74418515-G-C

364875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74418418-G-A

364945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74418345-A-G

365030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74418267-T-C

365313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74418021-T-G

365362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74417970-C-T

366135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74417398-T-G

http://identifiers.org/hco/5/GRCh38#366233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74417318-A-C

366313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74417259-C-T

366461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74417102-C-G

366612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74416961-G-A

366618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74416955-T-G

366687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74416875-C-G

366687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74416875-C-T

366715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74416844-C-G

367073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74416558-T-C

367225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74416453-G-A

367653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

367705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

http://identifiers.org/hco/5/GRCh38#367706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

367706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/5/GRCh38#367734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

367734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

367736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

367736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

http://identifiers.org/hco/5/GRCh38#367745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

367745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

367745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

367826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: -C-T

367887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: -C-T

367976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: -G-A

http://identifiers.org/hco/5/GRCh38#367999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

367999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

368034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

368284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74412073-A-G

368332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74412029-C-T

http://identifiers.org/hco/5/GRCh38#368432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74411902-C-A

368481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74411856-T-C

368640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74411703-C-T

368689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74411652-C-T

368704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74411637-A-G

368856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74411516-T-G

368875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74411497-G-T

368895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74411484-G-C

370803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74411200-G-A

394929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74395371-G-A

394937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74395363-G-A

395041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74395281-G-A

395060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74395266-G-A

395164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74395179-G-A

395208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74395146-C-T

395282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74395074-G-A

395317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74395039-C-T

http://identifiers.org/hco/5/GRCh38#395537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74394865-C-A

395594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74394811-C-T

395641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74394761-G-A

395641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74394761-G-C

395770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74394609-A-G

395889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74394453-G-T

395936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74394433-C-T

396068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74394325-C-T

396077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74394316-A-G

400047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74393849-C-T

400119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74393780-A-G

400236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74393629-T-C

400405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74393476-T-C

400459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74393424-G-T

401237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74392622-G-C

401237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74392622-G-T

401461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74392423-C-T

401620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74392283-G-A

401741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74392183-T-C

402089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74391881-C-T

402152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74391817-T-C

http://identifiers.org/hco/5/GRCh38#411558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74381523-C-A

412064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74379157-T-A

412146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74379100-C-T

413226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74378202-A-G

413259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74378182-T-C

413260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74378181-G-A

413260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74378181-G-T

http://identifiers.org/hco/5/GRCh38#413306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74378130-C-A

413306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74378130-C-G

413306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74378130-C-T

413477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74377969-T-C

421908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74373760-T-A

422009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74373654-G-A

422091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74373568-C-T

http://identifiers.org/hco/5/GRCh38#422192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74373472-C-A

422313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74373357-G-T

422441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74373269-G-A

422511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74373219-G-A

422511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74373219-G-T

422565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74373168-G-A

422632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74373100-A-G

422637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74373093-T-A

422637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74373093-T-C

422697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74373042-A-G

422703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74373036-G-T

http://identifiers.org/hco/5/GRCh38#422846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74372894-C-A

422849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74372891-T-C

422862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74372878-G-A

422862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74372878-G-T

http://identifiers.org/hco/5/GRCh38#423480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74371566-C-A

423480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74371566-C-T

423685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74371369-T-C

423749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74371321-T-A

423749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74371321-T-C

http://identifiers.org/hco/5/GRCh38#423754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74371316-C-A

423754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74371316-C-T

423776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74371287-G-A

423776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74371287-G-C

423776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74371287-G-T

423873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74371122-G-A

423873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74371122-G-T

424037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74370968-G-A

427288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74369220-C-T

427421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74369093-C-T

427465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74369051-G-A

427746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74368895-T-C

427760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74368881-C-T

427930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74368734-G-A

427930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74368734-G-T

http://identifiers.org/hco/5/GRCh38#428075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74368600-C-A

428075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74368600-C-G

428086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74368589-G-A

428086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74368589-G-T

428089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74368586-T-C

http://identifiers.org/hco/5/GRCh38#428097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74368578-C-A

428097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74368578-C-G

432171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74364263-T-A

432171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74364263-T-G

http://identifiers.org/hco/5/GRCh38#432275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74364147-C-A

http://identifiers.org/hco/5/GRCh38#432329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74364060-A-C

432329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74364060-A-G

432370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74363990-G-T

432371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74363989-T-C

432560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74363823-T-C

432616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74363771-G-A

432762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74363670-C-T

432767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74363665-C-G

432767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74363665-C-T

http://identifiers.org/hco/5/GRCh38#432790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74363643-C-A

432790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74363643-C-G

432790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74363643-C-T

432918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74363515-C-G

432918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74363515-C-T

432928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74363508-G-A

432928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74363508-G-C

432928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74363508-G-T

http://identifiers.org/hco/5/GRCh38#432991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74363448-A-C

432991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74363448-A-G

433299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74363256-C-T

433388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74363197-A-G

433442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74363149-T-G

433703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74362935-G-C

http://identifiers.org/hco/5/GRCh38#433776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74362858-C-A

433776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74362858-C-T

http://identifiers.org/hco/5/GRCh38#433797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74362845-C-A

433797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74362845-C-T

http://identifiers.org/hco/5/GRCh38#433874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74362761-C-A

433874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362761-C-G

433874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74362761-C-T

433973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74362629-T-C

434034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362571-G-A

434095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362501-C-T

434143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362453-T-C

http://identifiers.org/hco/5/GRCh38#434145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74362451-C-A

434145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362451-C-T

434151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362445-G-A

434176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362420-C-T

434221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362375-A-G

434238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362358-T-G

434249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74362347-G-A

434249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362347-G-T

http://identifiers.org/hco/5/GRCh38#434274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74362322-C-A

434295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362301-C-G

434295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362301-C-T

434314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362282-C-T

434315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74362281-G-A

434355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362241-T-C

434475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362115-C-T

434476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362114-G-A

434476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74362114-G-T

434622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74361989-T-C

http://identifiers.org/hco/5/GRCh38#434623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/13/GRCm39#74361988-C-A

434623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74361988-C-T

434707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74361901-A-G

http://identifiers.org/hco/5/GRCh38#434740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74361868-C-A

434740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74361868-C-G

434740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74361868-C-T

434818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74361790-G-A

434818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74361790-G-C

434818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74361790-G-T

434963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361683-A-G

http://identifiers.org/hco/5/GRCh38#434998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74361649-C-A

434998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361649-C-T

435020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361627-A-G

http://identifiers.org/hco/5/GRCh38#435024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74361623-C-A

435024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361623-C-T

435057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361596-T-A

435057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361596-T-C

435057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361596-T-G

435351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361507-G-A

435351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361507-G-T

435414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361492-T-C

435414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361492-T-G

435417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361489-G-A

435417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361489-G-T

435484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361468-T-G

435526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361426-A-G

435526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361426-A-T

435528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361424-T-A

435528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361424-T-C

435528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361424-T-G

435558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361408-G-C

435558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361408-G-T

435602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361367-G-A

435624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361345-A-G

435730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361263-G-C

435735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361258-G-A

435735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361258-G-T

435880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361120-T-C

435914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361085-A-G

http://identifiers.org/hco/5/GRCh38#435990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74361005-C-A

435990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361005-C-T

435994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74361001-T-C

436038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360978-A-G

436038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360978-A-T

436039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360977-A-G

436069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360969-G-A

436163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360878-C-T

436331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360816-G-A

436331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360816-G-C

http://identifiers.org/hco/5/GRCh38#436353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74360794-C-A

436400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360753-G-A

436433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360720-G-T

436481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360688-G-C

436481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360688-G-T

436527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360644-A-G

http://identifiers.org/hco/5/GRCh38#436632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74360591-C-A

436775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360458-G-A

436775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360458-G-T

436777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360456-G-A

436898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360399-C-T

436924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74360376-A-G

http://identifiers.org/hco/5/GRCh38#436991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74360321-C-A

437529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359915-A-G

437574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359881-G-T

437591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359871-T-A

437591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359871-T-C

http://identifiers.org/hco/5/GRCh38#437596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74359866-C-A

437596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359866-C-T

437678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359796-T-A

437678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359796-T-G

437682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359792-G-T

437683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359791-G-A

437683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359791-G-T

http://identifiers.org/hco/5/GRCh38#437745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74359711-C-A

437745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359711-C-T

437787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359669-G-T

437976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359516-T-C

437999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359492-T-C

438073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359417-C-G

http://identifiers.org/hco/5/GRCh38#438085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74359405-C-A

438085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359405-C-T

438164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359352-A-G

438274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 346
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74359234-G-T