22447660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, undefined
orthologous variants: 136781681-G-T

http://identifiers.org/hco/1/GRCh38#22447809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136781543-A-C

22447809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron variant
orthologous variants: 136781543-A-G

22447912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron variant
orthologous variants: 136781441-G-C

22448297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron variant
orthologous variants: 136781074-C-T

22449731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron variant
orthologous variants: 136777939-C-T

22450366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron variant
orthologous variants: 136777665-T-G

22450410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron variant
orthologous variants: 136777621-C-T

22450645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, undefined
orthologous variants: 136776843-A-G

22450754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron variant
orthologous variants: 136776751-T-C

22450811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron variant
orthologous variants: 136776696-A-G

22450876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron variant
orthologous variants: 136776631-C-T

http://identifiers.org/hco/1/GRCh38#22451775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#136776189-C-A

22451775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, undefined
orthologous variants: 136776189-C-T

http://identifiers.org/hco/1/GRCh38#22451798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#136776149-C-A

http://identifiers.org/hco/1/GRCh38#22452061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#136775897-C-A

22452061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136775897-C-T

22452161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136775777-G-T

22452216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136775724-G-A

22452226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136775717-C-T

22452380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136775654-C-G

22452414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136775625-C-G

22452479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136775576-G-A

22452479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136775576-G-C

http://identifiers.org/hco/1/GRCh38#22452567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136775470-A-C

http://identifiers.org/hco/1/GRCh38#22452641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136775392-C-A

http://identifiers.org/hco/1/GRCh38#22452676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#136775360-C-A

22452676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136775360-C-T

http://identifiers.org/hco/1/GRCh38#22452799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136775335-A-C

http://identifiers.org/hco/1/GRCh38#22452802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136775329-C-A

22452845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136775291-G-A

22452845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136775291-G-T

22453079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136775114-G-A

22453079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136775114-G-T

http://identifiers.org/hco/1/GRCh38#22453085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136775108-C-A

22455145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136772657-A-G

http://identifiers.org/hco/1/GRCh38#22455373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136772174-A-C

22455689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136771848-T-C

22455689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136771848-T-G

22455780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136771758-G-A

22455804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136771734-G-A

22455940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136771594-G-C

22455941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136771593-T-C

http://identifiers.org/hco/1/GRCh38#22455952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136771582-C-A

22455958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136771576-T-C

22456251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136771286-G-A

22456826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136770734-T-A

22460833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136768937-T-C

22460859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136768918-A-G

22461157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136768664-T-C

22461183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136768637-C-G

22461354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136768478-G-A

22461354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136768478-G-T

22461857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136767986-A-G

22461871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136767972-A-T

22461954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136767750-G-A

22462697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136766558-T-C

22462790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136766460-T-C

22462903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136766350-A-G

22462999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136766238-T-G

22463253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136765994-G-A

22463253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136765994-G-T

22468320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136762115-T-A

22468425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136762016-T-C

22468426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136762015-C-T

http://identifiers.org/hco/1/GRCh38#22469993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136761788-C-A

22469993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136761788-C-T

22470232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136761549-T-C

22470240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136761541-G-A

22470303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136761366-A-G

22470377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136761286-T-G

http://identifiers.org/hco/1/GRCh38#22470442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136761220-A-C

22470511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136761152-G-T

22470626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136761051-C-T

22471067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136760689-T-C

22471538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136759651-A-G

22471911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136759397-G-A

22471924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136759384-T-C

22472527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136759154-A-G

22472527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136759154-A-T

22472665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136759031-A-G

22472674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136759022-G-A

22472830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136758861-C-T

22472842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136758849-C-G

22473322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136758369-T-A

22473428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136758259-G-T

22473665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136757858-G-C

22473670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136757853-T-C

22473904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136757640-C-T

22474002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136757542-T-C

22474052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136757509-G-C

22474204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136757364-C-T

22474205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136757363-G-A

22474360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136757233-C-T

http://identifiers.org/hco/1/GRCh38#22474821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136756780-C-A

22474821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136756780-C-T

22474850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136756751-G-T

22474905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136756700-G-A

22474925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136756682-G-A

http://identifiers.org/hco/1/GRCh38#22475213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136756505-A-C

22475465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136756351-C-G

22475465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136756351-C-T

22475546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136756313-A-G

22475641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136756225-T-A

22475671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136756195-T-G

22476162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136755818-T-C

22476666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136755619-T-C

22477363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136754948-C-T

22477950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136754785-C-T

22480205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136751719-C-T

22480361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136751582-G-A

22480454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136751503-G-C

22480739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136751357-T-G

22480793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136751313-A-G

22480848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136751266-T-A

22480867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136751247-C-T

22481204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136750946-T-C

22481281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136750870-A-G

22482143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136750037-A-G

22482157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136750023-G-T

22487013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136749614-G-A

22487095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136749546-G-A

22487544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136749178-G-A

22487571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136749153-C-T

22488018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136748750-G-A

22488024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136748744-C-T

22488632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136747610-T-G

22488690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136747561-T-G

22488759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136747496-T-G

22489539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136746445-A-G

22489607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136746387-T-C

22489742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136746255-G-T

http://identifiers.org/hco/1/GRCh38#22489748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136746249-C-A

22489748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136746249-C-G

22489748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136746249-C-T

http://identifiers.org/hco/1/GRCh38#22489760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136746237-A-C

22489760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136746237-A-G

22489760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136746237-A-T

22489814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136746138-T-G

22489842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136746118-T-C

22489907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136746065-G-A

22489907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136746065-G-T

22489938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136746039-G-T

22489960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136746018-C-G

22489960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136746018-C-T

22490117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136745861-G-C

22490315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136745663-G-A

22490337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136745641-C-T

22490561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136745417-G-A

22490602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136745376-T-G

http://identifiers.org/hco/1/GRCh38#22490615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136745363-A-C

22490617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136745361-T-C

22490617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136745361-T-G

22490709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136745290-T-G

22491117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136745021-G-A

22491117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136745021-G-T

22491121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136745017-T-C

22491131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136745006-A-G

22491131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136745006-A-T

22491332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136744787-G-A

http://identifiers.org/hco/1/GRCh38#22491670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136744313-A-C

22491670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136744313-A-G

22491670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136744313-A-T

22491682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136744262-G-A

22491682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136744262-G-T

22491930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136743977-T-G

22492201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136743732-C-T

22492286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136743573-G-A

22492357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136743498-A-T

22492408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136743466-C-T

22492414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136743460-C-G

22492623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136743296-A-G

22492681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136743235-A-G

22492772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136743144-C-G

22492779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136743131-T-C

22492889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136742979-A-G

22492917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136742954-A-G

http://identifiers.org/hco/1/GRCh38#22492937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136742929-C-A

http://identifiers.org/hco/1/GRCh38#22492958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136742906-C-A

22493211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136742503-C-G

22493976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136740786-G-T

22494147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136740615-A-G

22494343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136740457-A-G

22494477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136740402-T-A

22494580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136740306-T-C

22494739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136740183-G-A

22494800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136740154-G-A

22494800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136740154-G-C

22494897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136740083-C-T

22494935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136740046-A-G

22495089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136739869-C-G

22495093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136739865-T-A

22497149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136739439-C-T

22497263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136739326-A-G

22497343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136739252-T-G

22497514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136739089-A-G

22497514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136739089-A-T

22497689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136738920-G-A

22497803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136738830-C-G

22497903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136738726-C-T

22498047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136738510-C-T

22498153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136738431-G-T

22498321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136738099-C-T

22498478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136737973-A-G

22498778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136737691-T-A

22498778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136737691-T-G

22498939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136737554-A-T

22498966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136737527-A-G

http://identifiers.org/hco/1/GRCh38#22499180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136737318-C-A

22499275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136737229-A-G

22499403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136737037-T-C

22500304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136736288-A-G

22501032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136735577-G-C

22501032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136735577-G-T

22501033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136735576-G-A

22501033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136735576-G-C

22501212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136735408-A-G

22501451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136735243-T-C

22501559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136735139-G-A

22501713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136735015-G-A

22501713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136735015-G-T

http://identifiers.org/hco/1/GRCh38#22501758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136734989-C-A

22501758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136734989-C-G

22501758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136734989-C-T

22502262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136734526-A-G

22502451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136734337-T-C

22502822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136734078-G-A

22503156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136733776-T-C

22503231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136733705-G-C

22503830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136733172-C-G

22503830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136733172-C-T

22504266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136732763-C-T

22504325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136732719-A-G

22505025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136732150-C-T

22505237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136731975-A-G

22505941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136728808-T-G

22505960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136728790-G-A

22505961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136728789-A-G

http://identifiers.org/hco/1/GRCh38#22505981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136728769-C-A

22505981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136728769-C-T

22505984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136728766-G-A

22505984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136728766-G-T

22506022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136728729-T-G

22506087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136728664-G-A

22506220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136728531-G-A

22506220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136728531-G-C

22506337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136728413-T-G

22506343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136728407-A-G

22506547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136728236-A-G

22506622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136728169-A-G

22507066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136727775-G-A

22507078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136727763-T-C

22507094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136727749-C-T

22507376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136727505-A-G

22507615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136727296-G-A

22507983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136726939-T-A

22508224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136726721-T-A

22508238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136726707-T-C

22508249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136726696-T-C

22508663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136725874-C-G

22508663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136725874-C-T

22508702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136725835-A-T

22508707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136725830-G-A

22508831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136725713-T-C

http://identifiers.org/hco/1/GRCh38#22508974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136725383-C-A

22508974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136725383-C-T

http://identifiers.org/hco/1/GRCh38#22508989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136725368-A-C

22508989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136725368-A-G

22509034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136725326-G-A

22509176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136725187-G-A

22509176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136725187-G-C

22509176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136725187-G-T

22509204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136725159-G-A

22510136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 136724620-G-A

22510361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136724414-T-C

22510667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136724112-G-A

22511051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723618-T-C

22511068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723601-T-C

22511117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723557-A-G

22511117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723557-A-T

http://identifiers.org/hco/1/GRCh38#22511122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136723552-C-A

22511122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723552-C-T

22511123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723551-A-G

22511123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723551-A-T

22511194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136723487-T-C

22511228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136723453-C-T

22511299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136723382-A-G

22511388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723302-C-T

22511392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723298-A-G

22511424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723264-A-G

22511424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723264-A-T

http://identifiers.org/hco/1/GRCh38#22511428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136723260-C-A

22511437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723251-T-C

22511491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723200-A-T

22511638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723054-G-T

22511639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723053-A-G

22511649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723046-G-A

22511651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136723044-G-A

22511669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 136723028-T-C

22511683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136723014-T-C

22511752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136722948-A-G

http://identifiers.org/hco/1/GRCh38#22511769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136722925-C-A

22511815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136722879-T-C

22511834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136722860-C-G

22511897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136722797-G-A

22511897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136722797-G-T

22512014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136722680-C-G

22512125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136722569-C-T

22512182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136722526-A-G

22512183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136722525-T-C

22512250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136722466-A-G

22512441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136722293-T-G

22512834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136721949-G-A

22512834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136721949-G-T

22512873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136721908-A-G

22512877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136721904-T-C

22512977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136721807-G-C

22513138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 136721649-G-A

22513167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136721621-T-A

22513167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136721621-T-C

22513167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136721621-T-G

22517000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136719252-A-G

http://identifiers.org/hco/1/GRCh38#22517192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136719076-C-A

22517194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136719074-T-C

22517213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136719056-C-G

22517290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136718981-G-A

22517329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136718942-G-T

22517383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136718888-G-T

22517389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136718882-C-G

22517419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136718852-T-C

http://identifiers.org/hco/1/GRCh38#22517431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136718840-A-C

22517431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136718840-A-G

22517452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136718819-C-T

22517593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136718687-T-C

22517764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136718535-C-T

22517842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136718414-A-G

22518218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136717849-G-C

22518668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136717317-C-T

22518670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136717315-A-G

22518747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136717265-C-T

22518782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136717232-T-C

http://identifiers.org/hco/1/GRCh38#22518814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136717205-C-A

22518814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136717205-C-T

http://identifiers.org/hco/1/GRCh38#22518953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136717088-C-A

22518970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136717071-C-G

22518970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136717071-C-T

22518971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136717070-G-A

http://identifiers.org/hco/1/GRCh38#22518997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136717046-C-A

22518997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136717046-C-G

22519029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136717036-A-G

22519060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136717006-A-G

22519169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136716915-G-A

22519305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136716762-T-G

22519502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136716581-T-C

22519502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136716581-T-G

22519507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136716576-T-C

22519670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136716426-G-A

22519670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136716426-G-T

22519758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136716344-A-G

http://identifiers.org/hco/1/GRCh38#22519766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136716338-A-C

22519766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136716338-A-T

22519823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136716281-G-A

22519823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136716281-G-T

http://identifiers.org/hco/1/GRCh38#22519858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136716247-C-A

22519858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136716247-C-G

22519858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136716247-C-T

http://identifiers.org/hco/1/GRCh38#22519948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136716171-C-A

22519964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136716158-G-C

http://identifiers.org/hco/1/GRCh38#22519982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136716140-C-A

22519982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136716140-C-G

22520037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136716091-C-T

22520038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136716090-T-C

22520111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136716021-C-T

22520210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136715922-C-T

22520219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136715913-G-T

22520372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136715778-T-C

22520568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136715377-A-G

22520791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136715190-G-T

22520907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136715100-G-A

22521002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136715016-G-A

22521165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136714890-T-C

22521205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136714849-G-A

22521228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136714826-C-T

22521269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136714793-C-T

22521544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136714632-T-C

22521679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136714514-G-A

22521689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136714504-G-A

22522149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136714072-C-T

22522150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136714071-A-T

22522220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136714006-G-T

22522261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713970-T-C

22522284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713950-G-A

22522284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713950-G-T

http://identifiers.org/hco/1/GRCh38#22522294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136713941-C-A

22522294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713941-C-T

22522301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713934-A-T

22522308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713927-T-G

http://identifiers.org/hco/1/GRCh38#22522317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136713918-A-C

22522317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713918-A-T

22522318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713917-G-A

22522318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713917-G-T

22522328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713906-G-A

22522391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136713864-G-A

22522424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136713831-C-G

http://identifiers.org/hco/1/GRCh38#22522479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136713777-A-C

22522479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713777-A-T

22522482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713774-A-G

22522507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713748-T-C

22522513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713742-T-C

http://identifiers.org/hco/1/GRCh38#22522537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136713718-C-A

22522537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713718-C-T

http://identifiers.org/hco/1/GRCh38#22522584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136713676-C-A

http://identifiers.org/hco/1/GRCh38#22522590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136713671-A-C

22522604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713660-T-A

22522619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713645-A-G

22522686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713580-A-G

http://identifiers.org/hco/1/GRCh38#22522797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136713490-A-C

22522797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713490-A-G

http://identifiers.org/hco/1/GRCh38#22522927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136713416-C-A

22522927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713416-C-T

22522985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713386-T-C

22523017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713354-G-A

22523017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713354-G-T

22523401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136713097-C-T

22523571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136712964-G-A

22523823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136712723-C-G

22524135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136712405-T-C

22524147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136712393-G-C

22524147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136712393-G-T

22524304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136712263-A-G

22524453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136712114-G-A

22524461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136712106-C-G

http://identifiers.org/hco/1/GRCh38#22524490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136712078-C-A

22524490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136712078-C-T

http://identifiers.org/hco/1/GRCh38#22524527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136712044-C-A

22524529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136712042-G-A

http://identifiers.org/hco/1/GRCh38#22524537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136712034-C-A

22524537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136712034-C-T

http://identifiers.org/hco/1/GRCh38#22524568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136711993-C-A

22524568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136711993-C-T

22524750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136711832-C-T

22524828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136711676-G-A

22524858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136711650-C-T

22524955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136711586-C-T

22524956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136711585-C-G

22525302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136711277-G-A

22525405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136711175-G-A

22525408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136711172-C-T

22525484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136711085-G-T

22525599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136711019-T-C

22525599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136711019-T-G

22526229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136710526-C-G

22526232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136710523-A-G

22526349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136710406-G-A

http://identifiers.org/hco/1/GRCh38#22526504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136710282-C-A

22526504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136710282-C-T

22526585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136710206-T-C

http://identifiers.org/hco/1/GRCh38#22526624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136710164-C-A

22526624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136710164-C-T

22526697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136710097-G-T

22526778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136710015-G-A

22526778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136710015-G-T

22526825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709975-G-A

22526874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709937-T-G

22527191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709674-T-C

22527261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709610-T-C

22527308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709562-G-A

22527308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709562-G-T

http://identifiers.org/hco/1/GRCh38#22527316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136709548-A-C

22527326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709538-G-A

http://identifiers.org/hco/1/GRCh38#22527339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136709525-C-A

22527596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709270-G-T

http://identifiers.org/hco/1/GRCh38#22527621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136709245-C-A

22527621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709245-C-T

22527651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709216-C-T

22527663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709204-G-T

http://identifiers.org/hco/1/GRCh38#22527715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136709138-C-A

22527757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709095-G-A

22527757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709095-G-T

22527780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709074-A-T

22527793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709058-G-T

22527794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136709057-G-T

http://identifiers.org/hco/1/GRCh38#22527877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136708974-C-A

22527877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708974-C-G

22527877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708974-C-T

22527888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708963-G-A

http://identifiers.org/hco/1/GRCh38#22528131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136708765-C-A

22528131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708765-C-T

22528169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708731-G-T

22528180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708720-G-A

22528209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708688-C-T

22528458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708547-T-A

22528597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708442-T-C

22529045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708292-A-G

22529046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708291-G-T

22529076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708261-A-G

22529264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708150-C-G

22529264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708150-C-T

http://identifiers.org/hco/1/GRCh38#22529280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136708136-C-A

22529280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708136-C-T

22529368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708068-G-A

22529368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708068-G-T

22529433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708012-G-A

22529433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136708012-G-C

http://identifiers.org/hco/1/GRCh38#22529494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136707987-C-A

22529593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707925-A-G

http://identifiers.org/hco/1/GRCh38#22529612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136707909-A-C

22529707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707835-C-G

22529722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707820-G-A

22529722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707820-G-T

22529729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707810-G-T

22529773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707768-A-G

http://identifiers.org/hco/1/GRCh38#22529789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136707754-C-A

22529789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707754-C-T

http://identifiers.org/hco/1/GRCh38#22529823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136707720-C-A

22529823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707720-C-G

22529823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707720-C-T

22529826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707717-G-A

22529826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707717-G-T

22529944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707665-A-T

http://identifiers.org/hco/1/GRCh38#22529976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136707653-C-A

22530079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707592-A-G

http://identifiers.org/hco/1/GRCh38#22530117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136707555-C-A

22530117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707555-C-T

22530171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707508-G-A

22530171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707508-G-C

22530171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707508-G-T

http://identifiers.org/hco/1/GRCh38#22530173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136707506-C-A

22530173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707506-C-T

22530247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707448-G-T

22530284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707410-A-G

22530381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707324-G-A

22530381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707324-G-T

http://identifiers.org/hco/1/GRCh38#22530402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136707304-C-A

22530642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707090-T-C

22530678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 136707055-G-T

22530784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3 prime UTR variant
orthologous variants: 136707004-G-A

22530859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3 prime UTR variant
orthologous variants: 136706962-T-G

http://identifiers.org/hco/1/GRCh38#22531061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136706873-C-A

22531061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3 prime UTR variant
orthologous variants: 136706873-C-T

http://identifiers.org/hco/1/GRCh38#22531063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29045
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136706871-C-A