138161956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 18619461-G-A

138161956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 18619461-G-T

http://identifiers.org/hco/6/GRCh38#138162305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18619160-A-C

138162305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18619160-A-T

http://identifiers.org/hco/6/GRCh38#138162311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18619154-A-C

138162825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18618629-G-A

138162999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18618504-C-T

138163082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18618406-T-C

138163577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18617885-G-T

http://identifiers.org/hco/6/GRCh38#138164166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18617330-C-A

138164248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18617247-G-A

138164248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18617247-G-C

138164288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18617205-C-T

http://identifiers.org/hco/6/GRCh38#138164580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18616941-C-A

138164580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18616941-C-T

138164841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18616722-T-A

138164874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18616704-C-G

138164893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18616685-T-C

138164907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18616672-G-A

138165824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18615035-G-A

138166210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18614716-T-A

138166324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18614605-A-G

138166585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18614168-G-A

http://identifiers.org/hco/6/GRCh38#138166654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18614113-A-C

http://identifiers.org/hco/6/GRCh38#138167108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18613725-A-C

138167484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18613513-C-T

138167513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18613499-C-G

138167544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18613480-A-G

138167673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18613365-T-C

138167677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18613361-T-G

138167865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18613169-G-A

http://identifiers.org/hco/6/GRCh38#138168027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18613055-A-C

138168086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18612996-T-C

138168416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18612651-G-A

138169685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18611065-C-G

138169688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18611062-T-C

138169751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18610999-T-C

138169909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18610846-C-T

http://identifiers.org/hco/6/GRCh38#138169916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18610839-A-C

138170145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18610634-T-C

http://identifiers.org/hco/6/GRCh38#138170192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18610472-A-C

138170432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18610067-G-T

138170558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18609968-A-G

138170573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18609958-G-A

http://identifiers.org/hco/6/GRCh38#138170593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18609939-A-C

138170619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18609898-G-A

138170619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18609898-G-C

138170619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18609898-G-T

138170664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 18609853-A-G

http://identifiers.org/hco/6/GRCh38#138170726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18609791-C-A

138170726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18609791-C-T

138171420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18609468-C-T

138172110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18608783-T-C

138172111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18608782-C-G

138172840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18608116-G-A

138172964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18607982-T-A

138173092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18607852-T-C

138173181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18607763-A-G

138173220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18607717-A-G

138173229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18607708-T-C

138173317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18607625-C-T

138173318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18607624-G-A

138173318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18607624-G-C

138173814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18607013-G-C

138173881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606952-C-G

138173971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606876-A-G

138174062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606793-T-C

138174091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606771-A-T

138174221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606648-G-A

138174235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606633-C-T

138174258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606608-T-C

138174271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606595-A-G

138174284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606582-A-G

138174311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606555-A-G

138174523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606525-T-A

138174523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606525-T-C

138174715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606429-G-A

138174724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606420-A-G

http://identifiers.org/hco/6/GRCh38#138175052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18606129-C-A

138175231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606056-A-G

138175243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606044-A-T

138175262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18606025-G-T

138175364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18605929-G-T

138175367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18605928-A-G

138175578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18605737-G-C

138178516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18603902-C-T

138178938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18603498-C-T

138179125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18603181-G-C

138179171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18603132-A-G

138179289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18603019-T-C

138179362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18602947-C-T

http://identifiers.org/hco/6/GRCh38#138179767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18602554-C-A

138180059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18602215-C-T

138180263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18602064-C-T

138180274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18602051-A-T

138180384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18601961-C-T

138180541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18601792-G-A

138180548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18601785-G-T

138180738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18600078-G-A

138181917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18599241-C-T

138182126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18598499-C-T

138182785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18597822-G-T

138182954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18597670-T-C

138183069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18597549-C-T

138183112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18597507-G-A

138185567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18596966-G-A

138185585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18596948-T-G

http://identifiers.org/hco/6/GRCh38#138185703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18596832-C-A

138185735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18596777-C-T

138185864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18596654-G-A

138185902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18596613-G-A

138185943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18596571-G-A

138185943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18596571-G-T

138186070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18596459-A-T

http://identifiers.org/hco/6/GRCh38#138186228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18596300-A-C

138186228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18596300-A-G

138186235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18596293-A-G

138186401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18596129-T-C

138188491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18595192-G-A

138188539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18595158-A-G

138188624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18595087-G-A

138188675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18594924-C-G

http://identifiers.org/hco/6/GRCh38#138188699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18594900-A-C

138189323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18594293-T-A

138189582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18594044-A-G

138189582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18594044-A-T

138189606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18594025-C-T

138189732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18593895-A-G

138189732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18593895-A-T

138190147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18593479-T-A

138190403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18593220-T-C

138190415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18593208-A-G

138190447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18593183-C-T

138190464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18593160-A-G

138190718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18592911-C-T

138190971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18592670-T-A

138191497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18591828-A-G

138191720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18591630-A-G

138191766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18591586-G-A

138191766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18591586-G-T

138192045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18591398-G-A

138192045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18591398-G-C

138194373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18586976-C-T

138194472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18586880-A-T

138194497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18586855-G-A

138197843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18583404-G-A

138197861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18583386-G-A

http://identifiers.org/hco/6/GRCh38#138197893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18583354-C-A

138197893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18583354-C-T

http://identifiers.org/hco/6/GRCh38#138197936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18583310-C-A

138197978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18583268-T-C

138198018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18583228-T-C

138198179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18583090-C-T

138198261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18583007-T-G

138198524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18582733-G-A

138198551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18582712-C-T

138198650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18582624-G-A

138198684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18582590-C-T

138198712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18582563-A-G

http://identifiers.org/hco/6/GRCh38#138198724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18582551-C-A

138202274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18580414-A-G

138203203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18578017-C-G

138203203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18578017-C-T

138203269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18577951-G-C

138203561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18577645-T-C

138203646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18577576-A-G

http://identifiers.org/hco/6/GRCh38#138204556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18577306-A-C

138204582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18577280-T-A

138204647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18577221-T-G

138205158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18576721-A-G

138205230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18576658-G-A

138205230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18576658-G-T

138205255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18576633-G-T

http://identifiers.org/hco/6/GRCh38#138205699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18576202-A-C

138205782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18576115-G-A

138205782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18576115-G-C

http://identifiers.org/hco/6/GRCh38#138205937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18575968-C-A

138206630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18575582-G-A

138206633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18575579-A-G

138206945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18575303-T-C

138206959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18575240-G-A

138206959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18575240-G-T

http://identifiers.org/hco/6/GRCh38#138206995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18575203-C-A

138206995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18575203-C-T

138207018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18575180-T-A

138207018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18575180-T-C

http://identifiers.org/hco/6/GRCh38#138207055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18575143-C-A

138207109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18575089-T-A

138207140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18575058-A-G

http://identifiers.org/hco/6/GRCh38#138207143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18575055-C-A

138207143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18575055-C-T

138207236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18574964-A-T

http://identifiers.org/hco/6/GRCh38#138207306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18574909-C-A

138207343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18574877-T-C

138207670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18573956-C-G

138207670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18573956-C-T

138207698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18573928-A-G

138207769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18573863-A-G

138207869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18573813-G-C

138207900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18573784-A-G

138207912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18573772-T-C

138207938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18573746-T-A

138208469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18573327-G-T

138208682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18573180-A-G

138208786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18573091-G-A

138208952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18573013-G-C

138209046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18572929-T-G

138209577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18572591-G-A

http://identifiers.org/hco/6/GRCh38#138209773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18572549-C-A

138209773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18572549-C-G

138209773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18572549-C-T

138209774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18572548-G-A

138209774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18572548-G-C

138209774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18572548-G-T

138209801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18572521-T-C

138209804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18572518-A-G

http://identifiers.org/hco/6/GRCh38#138209813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18572510-C-A

138209813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18572510-C-T

http://identifiers.org/hco/6/GRCh38#138209849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18572473-C-A

http://identifiers.org/hco/6/GRCh38#138210003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18572337-C-A

138210003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18572337-C-G

138210003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18572337-C-T

http://identifiers.org/hco/6/GRCh38#138210091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18572249-C-A

http://identifiers.org/hco/6/GRCh38#138210149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18572179-C-A

138210149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18572179-C-T

138210224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18572103-G-A

138210235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18572092-T-C

138210325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18572044-C-T

138210376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18571993-T-A

138210410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18571958-T-C

138210802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18570876-G-A

138210854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18570825-G-T

138211109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18570476-T-C

138211184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18570406-G-A

138211228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18570373-A-G

138211285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18570326-C-T

138211362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18570252-T-C

138211417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18570194-C-T

138214089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18569639-T-A

138214101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18569627-C-G

http://identifiers.org/hco/6/GRCh38#138214255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18569472-A-C

138214624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18568136-A-G

138214810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18567954-G-A

138215155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18567595-G-A

138215204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18567550-G-A

138215221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18567533-C-T

138215587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18567048-G-A

138215596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18567017-C-G

138215707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18566904-A-G

138216370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18566536-T-A

138216370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18566536-T-C

138216396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18566510-A-T

http://identifiers.org/hco/6/GRCh38#138216456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18566452-C-A

138216460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18566449-G-A

138216463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18566446-T-C

138216595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18565733-C-T

138216674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18565666-C-T

138216690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18565645-G-A

138216716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18565620-T-C

138216719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18565617-G-T

138216750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18565586-C-T

138216795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18565541-A-G

138216836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18565504-A-G

138217079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18565262-C-T

138217104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18565239-T-C

http://identifiers.org/hco/6/GRCh38#138217150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18565194-A-C

138217150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18565194-A-G

138217324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18565016-A-G

http://identifiers.org/hco/6/GRCh38#138217334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18565005-C-A

138217340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18564999-T-A

138217396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18564915-T-C

http://identifiers.org/hco/6/GRCh38#138217397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18564914-C-A

138217400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18564911-A-T

http://identifiers.org/hco/6/GRCh38#138217553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18564001-A-C

138217570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18563971-G-T

138217625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18563920-G-A

http://identifiers.org/hco/6/GRCh38#138217634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18563911-C-A

138217634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18563911-C-T

138217639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18563906-G-A

138217639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18563906-G-T

http://identifiers.org/hco/6/GRCh38#138217680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18563866-C-A

138217680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18563866-C-T

http://identifiers.org/hco/6/GRCh38#138217776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18563755-A-C

138217847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18563693-A-G

138217847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18563693-A-T

http://identifiers.org/hco/6/GRCh38#138217860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18563680-C-A

138217860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18563680-C-G

http://identifiers.org/hco/6/GRCh38#138217914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18563633-C-A

http://identifiers.org/hco/6/GRCh38#138217927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18563621-C-A

138217927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18563621-C-T

138218019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 18563533-A-G

138218368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 18563042-A-G

138218389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 18563021-C-T

138218425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18562994-T-A

138218425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18562994-T-C

138218426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18562993-G-A

138218426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18562993-G-T

http://identifiers.org/hco/6/GRCh38#138218430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18562989-C-A

138218451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18562968-A-G

138218455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18562964-T-C

138218507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18562928-G-T

http://identifiers.org/hco/6/GRCh38#138218533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18562916-A-C

138218533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18562916-A-T

138218537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18562912-T-C

138218537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18562912-T-G

http://identifiers.org/hco/6/GRCh38#138218548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18562901-C-A

138218552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18562895-G-A

138218552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18562895-G-T

http://identifiers.org/hco/6/GRCh38#138218623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18562829-C-A

138218623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18562829-C-G

138218626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18562826-A-T

138218735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18562720-A-G

138218812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18562642-G-A

138221472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18561508-T-C

138221555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18561426-G-A

138221591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18561408-T-C

138221731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18561272-A-G

138221789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18561215-C-T

138221959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18561038-A-T

138222620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18560719-G-A

138222682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18560657-G-A

138222965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18560583-G-A

138223021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18560537-G-T

138223037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18560521-T-C

138223245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18560434-G-A

138223312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18560367-T-G

http://identifiers.org/hco/6/GRCh38#138223339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18560340-A-C

138223539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18560186-A-G

http://identifiers.org/hco/6/GRCh38#138223545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18560180-C-A

138223650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18560106-A-G

138223736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18560004-A-G

138223920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18559850-C-T

138224128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18559681-T-C

138224129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18559680-C-T

138224249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18559574-G-T

138224270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18559552-A-G

138224314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18559527-T-G

138224408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18559437-C-T

138224601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18559024-G-C

138224736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18558907-T-C

138224766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18558888-G-A

138225090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18558562-T-C

138225119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18558533-A-G

138225154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18558501-T-C

138226994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18557152-G-A

138227180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18556985-C-G

138227304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18556846-T-C

138227344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18556804-G-A

138227777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18556333-A-G

138227784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18556326-T-C

138227966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18556142-G-T

138227988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18556121-C-T

138228549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18555829-T-C

http://identifiers.org/hco/6/GRCh38#138228596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18555813-C-A

138228947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18555480-C-G

138229027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18555401-A-G

138229204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18555224-A-G

138229430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18554986-A-G

138229671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18554525-G-A

138229671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18554525-G-C

138229671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18554525-G-T

138229702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18554487-T-C

138229702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18554487-T-G

http://identifiers.org/hco/6/GRCh38#138229713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18554476-C-A

138229882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18553543-T-C

138229958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18553474-T-G

138229965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18553458-T-C

http://identifiers.org/hco/6/GRCh38#138229967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18553456-C-A

138229967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18553456-C-T

138229995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18553431-T-C

138230686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18552911-T-C

138230892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18552699-C-G

138232398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18544035-G-A

138232539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18543909-T-C

http://identifiers.org/hco/6/GRCh38#138232574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18543871-A-C

138232574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18543871-A-G

138232667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18543772-A-G

138232734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18543712-A-G

138232845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18543601-T-C

138232941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18543504-C-G

138233074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18543439-T-C

http://identifiers.org/hco/6/GRCh38#138234234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18542975-A-C

138237945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18541258-G-T

138238234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18541088-A-T

138238270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18541052-G-A

138238335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18540988-A-G

138238407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18540899-T-C

138238416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18540866-G-A

138238452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18540811-G-A

138238596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18540672-T-A

138238596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18540672-T-C

138238626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18540642-A-G

http://identifiers.org/hco/6/GRCh38#138238691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18540561-C-A

http://identifiers.org/hco/6/GRCh38#138238741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18540513-A-C

138238764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18540496-T-C

http://identifiers.org/hco/6/GRCh38#138238776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18540484-C-A

138238838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18540429-A-G

138238929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18540245-C-T

138239936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18539423-C-T

138240095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18539277-T-G

138240118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18539254-C-T

http://identifiers.org/hco/6/GRCh38#138240123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18539249-A-C

138240330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18539058-A-G

138240462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18538762-C-G

138240594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18538631-G-A

138240641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18538584-G-A

138241793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18538174-C-T

138241829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18538138-T-C

138241880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18538087-C-T

138241893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18538074-A-G

138241989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537984-A-G

138241996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537977-T-C

http://identifiers.org/hco/6/GRCh38#138242053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18537943-C-A

138242063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537933-C-T

138242434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537578-A-T

138242477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537536-G-A

138242600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537430-T-C

138242843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537242-C-T

138242856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537229-G-A

http://identifiers.org/hco/6/GRCh38#138242860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18537225-C-A

138242860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537225-C-T

138242897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537189-T-G

http://identifiers.org/hco/6/GRCh38#138242919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18537167-C-A

138242919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537167-C-G

138242919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537167-C-T

138243028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537061-A-G

138243049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537035-A-G

138243069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537014-G-A

138243069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18537014-G-T

138245347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18536570-A-G

138245391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18536529-C-T

138245432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18536499-T-G

138245468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18536464-G-A

138245468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18536464-G-T

138245486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18536448-A-G

138245542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18536392-G-A

138245543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18536391-T-A

http://identifiers.org/hco/6/GRCh38#138245625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18536313-C-A

138245625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18536313-C-T

138245629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18536309-G-A

138249987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18534895-C-G

138250165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18534710-G-A

138250425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18534464-A-G

138250475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18534412-G-T

138250743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18533505-G-T

138250769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18533480-G-A

138250964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18533289-G-C

138251045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18533214-G-A

138251401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18532860-T-A

138251515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18532738-A-G

138251598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18532596-C-G

138251605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18532589-G-A

138252025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18532189-T-A

http://identifiers.org/hco/6/GRCh38#138252173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18532040-C-A

138252480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18531778-A-G

138252773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18531524-T-A

138252807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18531496-T-C

138252928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18531392-G-T

138253368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18530517-G-A

138253392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18530493-C-G

138253392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18530493-C-T

138253428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18530452-A-G

138253690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18530216-G-T

http://identifiers.org/hco/6/GRCh38#138253761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18530158-C-A

138253761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18530158-C-T

http://identifiers.org/hco/6/GRCh38#138253792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18530136-C-A

138253882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 18530058-A-G

http://identifiers.org/hco/6/GRCh38#138253883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18530057-C-A

138253883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18530057-C-T

138253917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18530023-A-G

138253917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18530023-A-T

138254032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18529915-T-C

http://identifiers.org/hco/6/GRCh38#138254061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18529889-C-A

138254061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18529889-C-T

http://identifiers.org/hco/6/GRCh38#138254062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18529888-C-A

138254062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18529888-C-T

138254102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18529851-G-A

138254102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18529851-G-C

http://identifiers.org/hco/6/GRCh38#138255056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18529521-C-A

138255056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18529521-C-T

http://identifiers.org/hco/6/GRCh38#138255167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18529408-A-C

138255324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18528721-G-A

138255324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18528721-G-T

http://identifiers.org/hco/6/GRCh38#138255342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18528703-A-C

138255342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18528703-A-G

138255342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18528703-A-T

138255362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18528683-A-G

138255363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18528682-T-A

138255363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18528682-T-G

http://identifiers.org/hco/6/GRCh38#138255397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18528652-C-A

138255397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18528652-C-T

http://identifiers.org/hco/6/GRCh38#138255413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18528636-C-A

138255413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18528636-C-T

http://identifiers.org/hco/6/GRCh38#138255487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18528562-C-A

138255515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18528534-A-G

138255526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18528523-C-T

138255538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18528511-G-A

138255599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18528450-C-T

138255734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18528315-C-G

138255734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 18528315-C-T

138255770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 18528273-G-A

138255770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 18528273-G-C

138255770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 18528273-G-T

http://identifiers.org/hco/6/GRCh38#138255886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18528162-C-A

138255886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18528162-C-T

http://identifiers.org/hco/6/GRCh38#138259060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18527130-C-A

138259060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18527130-C-T

138259142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18527048-G-A

138259207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18526982-A-G

138259276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18526931-C-G

138260329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18526470-G-A

138260329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18526470-G-C

138260462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18526347-G-A

138260477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18526332-T-C

138261500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18523690-T-C

http://identifiers.org/hco/6/GRCh38#138261513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18523679-C-A

138261513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18523679-C-T

138261555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18523634-A-G

138261555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18523634-A-T

138261578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18523611-G-A

138261578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 18523611-G-T

http://identifiers.org/hco/6/GRCh38#138261632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18523557-C-A

138261632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18523557-C-T

138261645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18523544-A-G

138261661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18523527-G-T

138261666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18523522-T-C

138261666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18523522-T-G

138261714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18523466-G-T

138261745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18523438-T-C

138262577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18522930-T-C

138262577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18522930-T-G

138262632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18522874-T-C

http://identifiers.org/hco/6/GRCh38#138262642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18522864-C-A

http://identifiers.org/hco/6/GRCh38#138262654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18522852-C-A

138262654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18522852-C-T

138262663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18522843-A-T

138262735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18522771-G-T

138262816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18522690-G-A

138262849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18522657-C-T

138263026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18522480-A-G

138263206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18522312-A-G

138263278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18522240-G-C

138263293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18522225-T-C

138263503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18522015-A-G

http://identifiers.org/hco/6/GRCh38#138263533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18521985-C-A

138263617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18521901-T-C

http://identifiers.org/hco/6/GRCh38#138263643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18521884-C-A

138263643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18521884-C-T

138263651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18521876-T-C

138263677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18521852-A-G

http://identifiers.org/hco/6/GRCh38#138263689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18521841-C-A

138268475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18517239-T-C

138268515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18517201-A-G

138268779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18516938-T-G

138268864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18516863-A-G

138268872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18516855-G-T

138268993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18516731-C-T

http://identifiers.org/hco/6/GRCh38#138269099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18516627-C-A

138269148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18516534-C-T

138269149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18516533-C-G

http://identifiers.org/hco/6/GRCh38#138269307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18516390-C-A

138269307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18516390-C-T

138269375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18516325-A-G

138272988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18515616-A-G

138273156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18515496-A-T

138273245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18515410-A-G

138273416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18515225-A-G

138273465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18515172-T-G

138273542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18515094-G-A

138273562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18515067-A-G

138273885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18514734-T-G

138273932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18514687-T-C

138273949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18514670-A-G

138273978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18514638-A-G

138274057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18514568-C-G

138274057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18514568-C-T

138278412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511630-T-G

http://identifiers.org/hco/6/GRCh38#138278418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18511625-C-A

138278418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511625-C-T

138278489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18511554-C-G

138278489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18511554-C-T

138278643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511389-T-G

138278652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511381-G-A

138278652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511381-G-T

138278700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511337-G-A

138278700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511337-G-T

http://identifiers.org/hco/6/GRCh38#138278723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18511314-C-A

http://identifiers.org/hco/6/GRCh38#138278727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18511310-C-A

138278727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511310-C-T

138278736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511301-G-A

http://identifiers.org/hco/6/GRCh38#138278746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18511291-C-A

138278746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511291-C-T

138278749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511288-G-A

138278749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511288-G-T

138278759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511278-G-T

138279432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511206-C-T

138279500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511144-T-G

138279535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18511112-T-C

138279763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18510891-G-A

138279850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18510810-T-C

138279881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18510776-A-G

138279881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18510776-A-T

138279888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18510770-A-G

http://identifiers.org/hco/6/GRCh38#138279891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18510767-C-A

138279961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18510710-G-A

138279961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18510710-G-T

138280187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18510486-T-A

138280193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18510480-C-T

138280195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18510478-C-T

http://identifiers.org/hco/6/GRCh38#138280215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18510458-C-A

138280215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18510458-C-T

138280257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18510419-C-T

138280522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18510197-G-C

138280908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18510122-C-T

138281771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18509978-G-A

138281807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18509942-A-T

138281937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18509815-T-G

138282383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18509681-G-A

138282386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18509678-C-T

138282771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18509302-G-A

138282774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18509299-C-G

http://identifiers.org/hco/6/GRCh38#138283088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18509005-A-C

138283178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18508921-T-C

138283179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18508920-G-T

138283212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18508885-G-C

138284361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18507968-C-T

138284381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18507948-C-G

138284628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18507717-A-G

138284731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18507602-C-T

138285549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18507338-T-A

http://identifiers.org/hco/6/GRCh38#138285660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18507004-C-A

138285728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18506935-G-A

138285859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18506805-G-A

138285859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18506805-G-C

138285859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18506805-G-T

138285917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18506712-G-A

138285917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18506712-G-T

138285990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18506628-G-A

138285990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18506628-G-T

138286044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18506574-A-G

138286089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18506530-A-G

http://identifiers.org/hco/6/GRCh38#138286095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18506524-C-A

138286095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18506524-C-T

138286522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18506419-A-G

138286543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18506398-A-G

138286556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18506380-A-G

http://identifiers.org/hco/6/GRCh38#138286582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18506357-C-A

http://identifiers.org/hco/6/GRCh38#138286651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18506288-C-A

138286651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18506288-C-T

http://identifiers.org/hco/6/GRCh38#138286679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18506262-C-A

138286679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18506262-C-G

138286679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18506262-C-T

138286706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18506236-G-C

138286796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18506146-A-G

138286800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18506142-G-T

138286895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18506047-G-A

138286895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18506047-G-T

138286969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18505975-A-G

138286996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18505959-C-T

138287034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18505922-A-G

138287058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18505902-T-C

138287088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18505873-T-A

138287088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18505873-T-C

http://identifiers.org/hco/6/GRCh38#138287306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18505691-C-A

138287306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18505691-C-T

138287321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18505677-G-C

138287423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18505557-G-A

138287428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18505552-A-G

138287573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18505419-C-G

138287742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18505287-G-T

138287906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18505139-T-C

138287980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18505067-T-C

138288126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18504996-G-A

138288200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18504934-A-G

138288237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18504902-A-T

138288768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18504278-G-A

138288787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18504261-T-C

http://identifiers.org/hco/6/GRCh38#138288843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18504214-A-C

138288843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18504214-A-G

138288888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18504169-G-C

138288907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18504150-C-G

138288956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18504105-T-A

http://identifiers.org/hco/6/GRCh38#138289424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18503930-A-C

138289477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18503866-G-A

http://identifiers.org/hco/6/GRCh38#138289673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18503675-C-A

http://identifiers.org/hco/6/GRCh38#138289686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18503662-C-A

138289686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18503662-C-T

138289712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18503636-G-A

138289712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18503636-G-T

138289781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18503554-T-A

138289781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18503554-T-G

http://identifiers.org/hco/6/GRCh38#138289988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#18503346-C-A

138289988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18503346-C-G

http://identifiers.org/hco/6/GRCh38#138289994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#18503340-A-C

138289994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18503340-A-G

138289999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18503335-A-G

138290048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18503296-G-A

138290048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18503296-G-C

138290050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18503294-T-A

138290050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18503294-T-G

138290069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18503276-G-A

138290069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18503276-G-T

138290071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18503274-A-G

138290082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18503263-T-C

138290152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18503201-A-G

138290185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18503167-A-G

http://identifiers.org/hco/6/GRCh38#138290487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18502894-A-C

138290487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18502894-A-G

138290523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18502859-T-G

138290616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18502780-G-A

138290781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18502712-C-T

138290879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18502007-G-A

http://identifiers.org/hco/6/GRCh38#138291211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18501718-A-C

138291334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18501598-G-A

138291334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18501598-G-T

138291629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18501310-G-A

138291629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18501310-G-T

138291675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18501265-A-G

http://identifiers.org/hco/6/GRCh38#138291697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18501242-C-A

138291697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18501242-C-T

http://identifiers.org/hco/6/GRCh38#138291832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18501112-C-A

138291832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18501112-C-T

http://identifiers.org/hco/6/GRCh38#138291850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18501094-C-A

138291850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18501094-C-T

138291892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18501052-G-A

138291892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18501052-G-T

138291893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18501051-G-A

138292076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18500876-G-A

138292076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18500876-G-T

138292092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18500850-T-C

http://identifiers.org/hco/6/GRCh38#138292096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18500844-A-C

138292096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18500844-A-G

http://identifiers.org/hco/6/GRCh38#138292131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18500803-C-A

http://identifiers.org/hco/6/GRCh38#138292143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18500792-A-C

138292143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18500792-A-T

138292680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18499643-C-T

138292728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18499600-T-G

138292900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18499407-A-G

138292935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18499371-G-A

138293789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18497206-T-C

http://identifiers.org/hco/6/GRCh38#138293887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18497106-C-A

138294003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18496995-G-A

138294003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18496995-G-C

138294003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18496995-G-T

138294009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18496989-A-G

http://identifiers.org/hco/6/GRCh38#138294167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18496837-C-A

138294167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18496837-C-T

138294174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18496830-C-G

138294174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18496830-C-T

http://identifiers.org/hco/6/GRCh38#138294179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18496825-C-A

138294179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18496825-C-T

138294188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18496816-A-G

138294205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18496799-T-C

138296510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18495801-G-A

138296510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18495801-G-T

138296604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18495742-A-G

138296670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18495676-G-A

138296670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18495676-G-T

138296689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18495657-T-C

http://identifiers.org/hco/6/GRCh38#138296839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18495510-A-C

138296839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18495510-A-T

138296851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18495498-C-G

138296864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18495485-G-C

138297015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18495329-G-T

138297063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18495308-G-A

138297063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18495308-G-T

138297064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18495307-G-A

138297064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18495307-G-T

138297066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18495305-A-G

138297071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18495300-G-A

138297090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18495282-T-A

138297216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18495137-T-C

138297406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18494962-A-G

138297406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18494962-A-T

138297428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18494940-C-T

138297446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18494922-G-T

138297467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18494901-C-T

138297672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18494377-C-T

138297720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18494329-C-G

138297720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18494329-C-T

138297746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18494303-A-G

138297868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18493479-G-C

138298077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18493258-G-A

138298077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18493258-G-T

138298157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18493178-A-G

138298249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18493100-G-A

138298457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18492913-T-G

138298465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18492903-G-T

138298488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18492879-A-T

138298501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18492866-T-A

http://identifiers.org/hco/6/GRCh38#138298513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18492854-C-A

138298513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18492854-C-T

138298569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18492806-G-A

138298569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18492806-G-C

138298569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18492806-G-T

138298774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18492606-G-A

138298774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18492606-G-T

138298799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18492581-G-T

138307167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18489100-G-A

138307167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18489100-G-T

138307230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18489050-G-A

138307240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18489040-T-A

138307256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18489025-G-C

138307268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18489013-G-A

http://identifiers.org/hco/6/GRCh38#138307440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18488841-C-A

138307440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18488841-C-G

138307459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18488822-A-G

138307533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18488762-T-C

http://identifiers.org/hco/6/GRCh38#138307543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18488752-A-C

138307543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18488752-A-G

138307543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18488752-A-T

138307561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18488734-C-T

138307794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18488353-T-C

138307824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18488323-G-T

138307988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18488133-A-G

138308122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18488023-A-G

http://identifiers.org/hco/6/GRCh38#138308231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18487940-C-A

138308415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18487765-T-C

138308655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18487145-G-A

138308655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18487145-G-T

138308786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18487025-A-G

138308898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18486913-G-T

138310026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18485347-C-T

138310180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18485188-C-T

138310578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18484837-C-T

138310580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18484835-C-T

http://identifiers.org/hco/6/GRCh38#138310619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18484796-C-A

138311152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18484346-C-T

138311517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 18484060-G-A

138311517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 18484060-G-C

138311517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 18484060-G-T

138311520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18484057-T-C

138311521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18484056-G-A

138311521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18484056-G-C

138311521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18484056-G-T

138311551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18484026-G-A

138311551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18484026-G-C

http://identifiers.org/hco/6/GRCh38#138311600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18483978-C-A

138311600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18483978-C-T

138313405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18483863-T-C

138313584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18483742-T-C

138313675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18483661-T-C

138313867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18483463-A-G

138313971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18483363-T-C

138313997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18483338-T-G

138313999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18483336-A-G

138314894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18483243-A-G

138315111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18483063-A-G

138315257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18482922-A-G

138315542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18482666-T-C

138315972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18482596-A-G

http://identifiers.org/hco/6/GRCh38#138316934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18479586-A-C

138317103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18479429-T-A

138317103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18479429-T-C

http://identifiers.org/hco/6/GRCh38#138317129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18479404-C-A

138317129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18479404-C-T

138317134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18479399-T-C

138317137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18479396-T-A

138317137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18479396-T-C

http://identifiers.org/hco/6/GRCh38#138317163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18479371-A-C

138317170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18479364-A-G

138317253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 18479279-C-T

138317295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18479237-G-T

138317543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18478990-T-C

138317632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18478929-G-A

http://identifiers.org/hco/6/GRCh38#138317731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18478835-C-A

138317950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18478664-G-T

138318157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18477727-T-A

138318157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18477727-T-G

138318242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18477680-A-G

138318551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18477507-G-T

138318833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18476967-A-T

138318840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18476960-A-G

138319091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18476738-C-T

138319095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18476734-C-G

138319213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18476679-G-A

http://identifiers.org/hco/6/GRCh38#138319614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18476447-A-C

138319654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18476408-A-G

http://identifiers.org/hco/6/GRCh38#138319661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18476397-C-A

138319661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18476397-C-T

138319668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18476390-T-A

138319668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18476390-T-C

138319669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18476389-A-T

138319846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18476213-G-A

138319846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18476213-G-C

138319910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18476149-G-A

138320244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18475981-G-T

138320321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18475901-G-A

138320485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18475746-G-A

138320604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18475625-A-G

138320987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18475165-T-A

138320987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18475165-T-C

138320987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18475165-T-G

http://identifiers.org/hco/6/GRCh38#138320990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18475162-A-C

138320990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18475162-A-G

138321233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 18474924-A-G

138321233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 18474924-A-T

138321260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18474897-G-A

138321260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18474897-G-T

138321337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18474825-G-A

138321337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18474825-G-C

138321356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18474809-A-G

138323031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18473832-A-G

138323161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18473716-T-C

138323176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18473701-A-G

138323232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18473647-G-C

138323791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18473421-A-G

138323880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18473333-C-G

http://identifiers.org/hco/6/GRCh38#138323882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18473331-C-A

138323882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18473331-C-G

138323904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18473315-G-A

http://identifiers.org/hco/6/GRCh38#138323917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18473296-C-A

http://identifiers.org/hco/6/GRCh38#138323935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18473278-C-A

138324065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18473163-G-A

http://identifiers.org/hco/6/GRCh38#138324107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18473121-C-A

138324107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18473121-C-G

138324107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18473121-C-T

http://identifiers.org/hco/6/GRCh38#138324270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18472974-C-A

138324270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18472974-C-T

138324288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18472956-T-C

138324288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18472956-T-G

138327753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18471026-G-T

138327914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18470893-T-A

138328163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18470641-T-A

138328163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18470641-T-C

138328170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18470634-G-C

138328175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18470629-T-C

138328182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18470622-A-G

138328182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18470622-A-T

http://identifiers.org/hco/6/GRCh38#138328241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18470584-C-A

138328241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18470584-C-T

138328478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18470363-G-C

http://identifiers.org/hco/6/GRCh38#138328606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18470266-C-A

138328606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18470266-C-G

138328608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18470264-T-C

138328642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18470234-G-T

138330779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18469496-G-C

138332417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18469304-T-G

138332465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18469254-G-A

138332465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18469254-G-C

138333853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18468199-G-A

138333873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18468182-G-A

138333873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18468182-G-T

http://identifiers.org/hco/6/GRCh38#138333874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18468181-C-A

138333874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18468181-C-T

138333928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18468130-G-A

138333928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18468130-G-T

138334004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18468054-T-G

138334038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18468020-T-C

138334250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18467808-G-A

138334361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18467697-A-G

http://identifiers.org/hco/6/GRCh38#138334724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18467334-A-C

138334724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18467334-A-T

138334838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18467226-G-C

138334985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18467079-G-T

http://identifiers.org/hco/6/GRCh38#138335126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18466938-C-A

138335126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18466938-C-T

138335162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18466902-G-A

138335162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18466902-G-T

138335177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18466887-G-A

138335177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18466887-G-T

http://identifiers.org/hco/6/GRCh38#138335195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18466869-C-A

138335195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 18466869-C-T

138336282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18465531-T-C

138336295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 18465518-G-A

138336430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 18465383-C-T

http://identifiers.org/hco/6/GRCh38#138336575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18465252-C-A

138336575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18465252-C-T

138336715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18465116-T-C

http://identifiers.org/hco/6/GRCh38#138336721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18465110-A-C

138336788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18465050-G-T

http://identifiers.org/hco/6/GRCh38#138336850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18464989-C-A

138336928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18464916-T-C

138336928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18464916-T-G

http://identifiers.org/hco/6/GRCh38#138336994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18464855-A-C

http://identifiers.org/hco/6/GRCh38#138337069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18464773-A-C

138337069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18464773-A-G

138337075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18464767-A-G

138337075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18464767-A-T

http://identifiers.org/hco/6/GRCh38#138337218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18464632-C-A

138337402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18464470-A-G

138337501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18464353-G-A

138337501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18464353-G-T

138337987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18463815-G-T

138338005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18463798-T-C

138338056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18463750-A-G

138338252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18463468-G-T

138338303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18463419-A-T

138338451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18463289-A-G

138338865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18463150-A-G

138339141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18462939-G-A

138339141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18462939-G-T

138339226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18462858-G-T

138339256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18462828-A-G

138339543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18462550-A-G

138339545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18462548-A-G

http://identifiers.org/hco/6/GRCh38#138339610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18462497-C-A

138339610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18462497-C-T

138339769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18462280-A-G

http://identifiers.org/hco/6/GRCh38#138339808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18462244-C-A

138339834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18462220-T-C

138340711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18461407-A-G

138340829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18461286-A-G

138340829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18461286-A-T

138340889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18461223-G-A

http://identifiers.org/hco/6/GRCh38#138341008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18461141-C-A

138341008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18461141-C-T

138341152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18461009-T-C

http://identifiers.org/hco/6/GRCh38#138341267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18460900-C-A

138341315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18460856-A-G

138341336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18460835-T-G

http://identifiers.org/hco/6/GRCh38#138341399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18460788-C-A

138341787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18460459-T-C

138341809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18460435-A-G

138341967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18460246-A-G

138341971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18460242-A-G

http://identifiers.org/hco/6/GRCh38#138341982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18460231-A-C

138342079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18460167-T-C

http://identifiers.org/hco/6/GRCh38#138342131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18460103-C-A

138342273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18459988-G-T

http://identifiers.org/hco/6/GRCh38#138342353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18459932-C-A

138342355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18459930-G-T

http://identifiers.org/hco/6/GRCh38#138342389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18459902-C-A

138342441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18459850-T-C

138342574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18459728-T-C

138342658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18459651-C-T

138343183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18458996-G-T

138343259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18458861-T-C

138343490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18458668-C-T

138343492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18458666-A-G

138343697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18458489-G-A

138343893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18458299-T-C

138343904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18458289-G-A

138343904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18458289-G-T

138343919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18458274-G-A

138343919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18458274-G-T

138344008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18458164-G-A

http://identifiers.org/hco/6/GRCh38#138344009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18458163-C-A

138344009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18458163-C-T

http://identifiers.org/hco/6/GRCh38#138344098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#18458082-C-A

138344112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18458069-T-C

138344279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18457906-C-T