5421727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70787307-A-G

5422303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70786263-G-A

5422628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70785958-G-T

5422700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70785913-G-A

5422738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70785874-C-G

5422738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70785874-C-T

5422748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70785867-G-A

http://identifiers.org/hco/5/GRCh38#5422796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70785819-C-A

5422796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70785819-C-G

5422796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70785819-C-T

5423023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70785618-G-A

5423023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70785618-G-C

5423023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70785618-G-T

5423134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70785603-G-A

5423134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70785603-G-T

5423171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70785595-G-T

5423318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70785462-C-T

5423386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70785402-C-G

5423479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70785309-T-G

5423486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70785302-T-C

5424295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70784634-G-A

5424303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70784626-T-C

5424347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70784585-C-T

5424482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70784474-T-C

5424517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70784449-T-C

5424685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70784351-T-A

5424874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70784187-G-A

5424927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70784120-C-T

5424948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70784090-G-A

5425133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70783887-G-C

5425133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70783887-G-T

5426060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70783063-A-T

5426065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70783058-A-G

5434560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70779201-C-T

5436385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70772618-T-C

5436520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70772485-A-G

5436520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70772485-A-T

5437067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70772087-T-A

5437067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70772087-T-C

5437067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70772087-T-G

5437133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70772022-T-C

5437244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70771927-G-A

5437244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70771927-G-T

5437252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70771919-A-G

http://identifiers.org/hco/5/GRCh38#5437254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70771917-C-A

5437254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70771917-C-T

5437259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70771912-T-A

5437285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70771888-T-A

http://identifiers.org/hco/5/GRCh38#5437288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70771885-A-C

5437288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70771885-A-G

5437288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70771885-A-T

5437344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70771820-T-C

5437356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70771810-A-G

5438782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: -A-G

5438962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: -C-T

5439871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70769597-A-G

5439871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70769597-A-T

5439940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70769524-G-A

5439940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70769524-G-T

5440066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70769430-A-T

5440231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70769284-T-C

5440231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70769284-T-G

5440437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70769096-C-T

5441232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70768760-A-G

5441232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70768760-A-T

5441257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70768740-T-A

5441257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70768740-T-G

5441305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70768685-T-C

5441312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70768677-T-C

5441458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70768557-G-A

5441499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70768529-G-A

5441849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70768267-T-C

5441853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70768263-T-C

5441928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70768191-C-G

5441928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70768191-C-T

5442115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70768094-C-T

5442163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70768050-A-G

5442195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70768025-T-C

5442229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70767992-G-A

5442299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70767927-C-G

5442498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70767764-G-C

5442713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70767589-G-C

5443030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70767330-T-C

5443031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70767329-A-G

5443070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70767286-G-A

5443070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70767286-G-T

5443097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70767248-G-A

5443097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70767248-G-T

5443111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70767234-G-T

http://identifiers.org/hco/5/GRCh38#5443113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70767232-C-A

5443255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70767089-A-G

5443661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70766655-G-A

5443661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70766655-G-T

5443704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70766601-G-C

http://identifiers.org/hco/5/GRCh38#5443862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70766479-A-C

5443977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70765552-G-C

5444155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70765390-T-A

5444179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70765369-A-G

5444199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70765357-T-A

5444296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70765244-A-G

5444328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: splice donor variant
orthologous variants: 70765212-T-C

5446712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70763938-A-T

5446720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70763930-G-A

5446764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70763908-G-C

5446805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70763874-T-G

5446846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70763833-A-G

5447387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70763561-A-G

5447468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70763492-A-G

5447528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70763435-A-T

5447567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70763371-G-C

5447604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70763326-A-G

http://identifiers.org/hco/5/GRCh38#5447607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70763323-C-A

5447607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70763323-C-T

5447751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70763200-A-G

http://identifiers.org/hco/5/GRCh38#5447827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70763120-C-A

5447827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70763120-C-T

5447955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70762987-A-G

5448042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70762911-T-A

5449825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70761998-C-G

5449897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70761937-G-A

5449914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70761920-A-T

5450667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70761311-T-G

5451132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70760899-A-G

http://identifiers.org/hco/5/GRCh38#5452448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70760575-A-C

5452732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70760381-C-T

5452746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70760367-T-A

5452746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70760367-T-C

5453013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70760207-T-C

5453841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70759506-C-G

5453997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70759362-C-T

5454191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70759134-A-G

5454433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70758822-G-A

5454533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70758753-G-A

5454533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70758753-G-T

5454611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70758678-C-G

5454611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70758678-C-T

http://identifiers.org/hco/5/GRCh38#5454651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70758641-C-A

5454651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70758641-C-T

5454816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70758518-C-T

5454837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70758496-A-G

5454896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70758441-G-A

5457188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70757426-G-A

5457188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70757426-G-T

5457246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70757361-G-A

5457246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70757361-G-C

5457246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70757361-G-T

5457254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70757353-G-C

5457254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70757353-G-T

5457289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70757334-G-C

5457289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70757334-G-T

5457342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: 70757283-C-G

5457400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70757228-G-A

5457401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70757227-G-A

5457430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70757198-A-G

5457914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70756733-A-G

5459254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70755921-T-C

5459254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70755921-T-G

5459335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70755845-G-A

5459529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70755621-G-A

http://identifiers.org/hco/5/GRCh38#5460191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70755135-C-A

5460230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70755116-G-C

5460231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70755115-G-A

http://identifiers.org/hco/5/GRCh38#5460321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70755057-C-A

5460321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70755057-C-T

5460404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70755017-G-C

5460472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70754957-A-G

5460502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: stop gained
orthologous variants: 70754927-G-T

5460526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70754903-A-G

5460789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: 70754658-A-G

5461042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70754405-A-G

5461131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: 70754337-T-C

5461284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: 70754208-G-A

5461284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: 70754208-G-T

5461388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70754122-T-C

5461508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70753996-A-T

5461787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70753717-A-G

http://identifiers.org/hco/5/GRCh38#5461800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70753704-A-C

5461800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: 70753704-A-G

5461856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70753648-A-G

5461856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70753648-A-T

5461876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70753628-A-G

5461933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70753571-C-T

5461969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70753535-A-G

5462027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70753477-T-C

5462027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70753477-T-G

5462048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70753456-A-G

5462048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70753456-A-T

5462191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70753313-A-G

http://identifiers.org/hco/5/GRCh38#5462211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70753293-C-A

5462211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: 70753293-C-T

5462233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: stop gained
orthologous variants: 70753271-C-T

5462357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70753165-T-G

5462523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: 70753014-T-C

5462550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: 70752987-T-A

http://identifiers.org/hco/5/GRCh38#5462596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70752941-A-C

5462596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70752941-A-G

5462644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70752893-G-A

5462690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70752817-G-A

5462710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70752797-C-G

5462710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70752797-C-T

5462848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70752659-A-T

5462899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70752608-T-A

http://identifiers.org/hco/5/GRCh38#5462956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70752551-A-C

5462956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70752551-A-G

5463171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: 70752333-T-G

5463269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70752235-C-T

http://identifiers.org/hco/5/GRCh38#5463297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70752207-A-C

5463297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: 70752207-A-G

5463382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70752125-T-A

5463499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70752008-G-A

5463499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70752008-G-C

5463511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70751996-A-G

http://identifiers.org/hco/5/GRCh38#5463710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70751797-C-A

5463750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: 70751772-G-A

5463762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: 70751760-T-A

http://identifiers.org/hco/5/GRCh38#5464011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70751511-A-C

5464044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: synonymous variant
orthologous variants: 70751478-T-C

5464108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70751414-G-A

http://identifiers.org/hco/5/GRCh38#5464153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70751369-A-C

5464308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70751214-T-A

5464370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70751152-C-T

5464462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70751060-G-C

5464462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70751060-G-T

http://identifiers.org/hco/5/GRCh38#5464471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70751051-C-A

5464936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70750583-C-T

5464937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70750582-A-G

5465257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70750257-G-A

5465257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70750257-G-T

5465281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70750239-A-G

5465281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70750239-A-T

5465312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70750221-G-T

http://identifiers.org/hco/5/GRCh38#5465325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70750208-A-C

5465417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70750136-G-A

5465492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70750083-C-T

5466021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70749614-A-G

5468751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70747405-T-A

5468751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70747405-T-C

5468756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70747400-T-C

5468756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70747400-T-G

5468857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70747298-T-C

5469014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70747114-G-A

5469014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70747114-G-T

5469084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70746848-G-A

5469084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70746848-G-T

5469158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70746745-T-A

5469327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70746592-A-G

5472189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70745495-C-T

5473172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70744724-G-A

5473299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70744621-G-A

5473412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70744546-A-G

5473434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70744526-T-C

5473440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70744520-A-G

5473440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70744520-A-T

http://identifiers.org/hco/5/GRCh38#5473618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70744402-C-A

5473618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70744402-C-T

5473684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70744336-A-G

5473828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70744197-T-C

5473891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70744150-A-G

5473891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70744150-A-T

5475931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 70743087-A-G

5476025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70742996-G-A

5476025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70742996-G-T

http://identifiers.org/hco/5/GRCh38#5486891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70740651-C-A

http://identifiers.org/hco/5/GRCh38#5486895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70740647-C-A

5486895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70740647-C-T

5486963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70740615-A-G

5487236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70740286-A-G

5487514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: 70740034-C-T

http://identifiers.org/hco/5/GRCh38#5489089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70737992-C-A

5489271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70737807-T-G

5489281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: missense variant
orthologous variants: 70737797-T-C

http://identifiers.org/hco/5/GRCh38#5489360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70737701-C-A

5489360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: 3 prime UTR variant
orthologous variants: 70737701-C-T

5489458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: 3 prime UTR variant
orthologous variants: 70737581-G-T

http://identifiers.org/hco/5/GRCh38#5489459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#70737580-C-A

5489825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: 3 prime UTR variant
orthologous variants: 70737210-A-G

5489838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29154
most severe consequence: 3 prime UTR variant
orthologous variants: 70737197-T-C