106991398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 84967598-T-C

http://identifiers.org/hco/12/GRCh38#106991639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84967817-C-A

http://identifiers.org/hco/12/GRCh38#106992387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84968597-C-A

http://identifiers.org/hco/12/GRCh38#106992427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84968633-A-C

106992442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84968647-T-A

http://identifiers.org/hco/12/GRCh38#106992480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84968665-C-A

106992486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84968671-T-C

106992560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84968720-T-C

106992571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84968732-T-A

106992572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84968733-G-T

106992594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84968759-G-A

106992594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84968759-G-T

http://identifiers.org/hco/12/GRCh38#106992614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84968771-C-A

106992614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84968771-C-G

106992614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84968771-C-T

106992646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84968803-A-G

106992702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84968835-A-T

106992703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84968836-G-T

106992706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84968839-T-C

106992710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 84968843-T-C

106992826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84968958-C-G

106992826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84968958-C-T

106992871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84969003-A-G

106992996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84969137-G-A

106993004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84969145-C-T

106993013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84969154-A-G

106993085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84969218-T-C

http://identifiers.org/hco/12/GRCh38#106993111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84969245-C-A

106993111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84969245-C-T

106993136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84969270-T-C

106993208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84969332-C-T

106993308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84970265-G-C

106993382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84970339-T-C

106993539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84970486-C-T

106993847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84976423-C-T

106994084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84976647-C-G

106994406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84976943-G-A

106994660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84977169-T-C

106994735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84977231-G-A

106995006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84977495-T-C

106995198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84977650-C-G

106995300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84977702-T-C

106995371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84977767-T-C

106996871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84978393-G-C

106997077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84978673-G-C

106997158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84978748-G-T

http://identifiers.org/hco/12/GRCh38#106997175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84978765-C-A

106997237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84978827-A-G

106997303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84978946-T-G

106997355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84979001-A-G

106997373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84979019-T-G

106997548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84979563-G-A

http://identifiers.org/hco/12/GRCh38#106997681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84979696-C-A

106997681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84979696-C-T

106997742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84979760-T-C

106997894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84980002-T-C

http://identifiers.org/hco/12/GRCh38#106997901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84980009-C-A

106997983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84980086-T-C

http://identifiers.org/hco/12/GRCh38#106998215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84980302-C-A

106998215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84980302-C-G

106998215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84980302-C-T

106998516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84981167-T-C

106999532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84982189-T-C

http://identifiers.org/hco/12/GRCh38#106999544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84982201-C-A

106999544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 84982201-C-T

106999546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84982203-C-G

106999620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84982277-T-C

106999867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 84982524-G-A

107000108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84982764-T-C

107000108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84982764-T-G

107000189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84982900-A-G

107000276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84982986-T-C

107001071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84983556-A-G

107001171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84983646-A-G

107001171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84983646-A-T

107001186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84983661-A-G

107001450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84983975-T-C

107001451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84983976-T-C

107001524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84984098-C-T

107001529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84984103-T-A

107001552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84984125-C-T

107001611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84984169-T-C

http://identifiers.org/hco/12/GRCh38#107001628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84984187-C-A

http://identifiers.org/hco/12/GRCh38#107001751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84984465-A-C

107001751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84984465-A-T

107001777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84984491-T-G

107001964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84984678-G-A

107001964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84984678-G-C

107001998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84984707-T-C

107002020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84984728-A-G

107002045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84984746-T-A

107002045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84984746-T-G

107002059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84984760-T-C

107002060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84984761-T-C

107002189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84984879-T-C

107004270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84986262-T-C

107004586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84986569-G-T

http://identifiers.org/hco/12/GRCh38#107004954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84986952-C-A

107004958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84986958-G-A

107004958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84986958-G-C

107005015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84987001-A-G

107005241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84987212-T-C

107005264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84987235-G-A

http://identifiers.org/hco/12/GRCh38#107005270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84987244-C-A

107005270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84987244-C-T

107005283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84987257-T-C

107005525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84987486-C-T

107005755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84987691-C-T

107005943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84987870-G-T

107006315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84988122-G-A

107006536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84988325-T-C

107007038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84988482-T-A

107007223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84988669-A-G

107007224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84988670-A-T

107007397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84988835-G-A

107007603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84988895-C-T

107007809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84988954-C-T

107007902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84989038-C-T

107007971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84989102-T-C

107007976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84989107-T-C

107008039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84989167-T-C

107008095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84989224-T-C

107008116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84989249-G-A

107008116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84989249-G-T

http://identifiers.org/hco/12/GRCh38#107008136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84989264-A-C

107008175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84989294-G-A

107020170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84990635-G-A

107020170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84990635-G-T

107020203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84990760-G-A

107020987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84991833-T-A

107021189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84992047-A-G

107021452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84992302-C-T

107021563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84992412-A-G

107021724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84992514-A-T

http://identifiers.org/hco/12/GRCh38#107021958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84992797-C-A

107022043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84992908-T-A

107022043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84992908-T-C

107022043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84992908-T-G

107022323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84993180-C-G

107022326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84993183-T-C

http://identifiers.org/hco/12/GRCh38#107022511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84993344-C-A

107022639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84993523-T-C

http://identifiers.org/hco/12/GRCh38#107022735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84993861-C-A

107022806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84993917-T-A

107022825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84993935-G-A

107023287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84994200-G-T

107023529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84994359-T-C

107023979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84994711-G-A

107024169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84995512-T-C

107024227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84995556-T-C

107025109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84995763-G-T

107025118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84995772-C-T

http://identifiers.org/hco/12/GRCh38#107025568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84996061-A-C

107025724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84996206-T-C

107025820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84996300-C-G

107025866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84996344-T-C

http://identifiers.org/hco/12/GRCh38#107025873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84996351-A-C

107026181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84996569-T-G

107026834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84997021-T-A

107026911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84997096-T-C

107027591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84997633-A-G

107027605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84997647-T-C

107027776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84997812-T-C

http://identifiers.org/hco/12/GRCh38#107028668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#84998774-C-A

107028668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84998774-C-T

107028677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84998783-A-G

107028945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84999055-A-G

107029664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84999253-T-G

107029863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84999429-A-G

107029936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84999500-G-C

107030292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85000002-T-A

107030362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85000079-T-C

107030952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85001634-G-A

107030952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85001634-G-C

http://identifiers.org/hco/12/GRCh38#107031322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85001970-C-A

107031404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85002010-T-A

107031404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85002010-T-C

http://identifiers.org/hco/12/GRCh38#107031458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85002065-C-A

107031520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85002122-T-C

107031718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85002538-T-C

107031894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85002711-A-G

107032339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85002811-C-T

107035263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85005670-T-G

107035338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85005752-T-C

107035389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85005801-G-C

http://identifiers.org/hco/12/GRCh38#107036025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85006707-C-A

107036123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85006814-T-C

107036151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85006838-T-A

107063977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85010434-C-T

107064089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85010531-T-C

107067496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85015431-A-G

107067801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85015745-C-T

107091650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85019081-C-G

107091650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85019081-C-T

107091807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85019219-G-A

107092099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85019521-T-C

107092393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85019804-T-G

107092621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85020004-G-A

107092767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85020137-A-T

107092878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85020252-G-C

107092917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85020291-G-A

107092941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85020315-G-A

107092974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85020347-G-A

107092974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85020347-G-T

107092983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85020367-T-C

107092983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 85020367-T-G

http://identifiers.org/hco/12/GRCh38#107093011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85020395-C-A

107093011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 85020395-C-T

107093150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 85020525-A-G

107093150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 85020525-A-T

http://identifiers.org/hco/12/GRCh38#107093257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85020626-C-A

107093257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 85020626-C-T

107093363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 85020732-G-A

107093363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 85020732-G-C

107093363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 85020732-G-T

107093416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85020776-G-A

107093416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 85020776-G-T

107093455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85020822-G-T

http://identifiers.org/hco/12/GRCh38#107093460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2384
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#85020827-A-C